Abstract: A formulation containing organic and non-organic ingredients that readily convert human, animal and bird excreta and/or bio hazard into biodegradable and/or nonbiodegradable gel or granules. Formulation comprises organic and / or inorganic ingredients; absorbent, biocide, binder, fragrance additive, anthelmintic, anti protozoal and bacterial culture. Formulation can be deployed in various forms or modes that may be placed in receptacles.
The present invention relates to a formulation that absorbs and converts human and animal excreta and bio hazards into a 99.99% germ free fragrant bio-degradable and/or non-biodegradable gel or granules.
BACKGROUND OF INVENTION
The factual challenges facing the world today are stated as hospital acquired infections (HAI), widespread contagious diseases (bacterial, viral, fungal, spores), zoonotic diseases and infected or non treated human, animal and bird excreta (and/or bio hazard) contaminating the living and natural environments which promotes proliferation of germs (pathogens), helminth and protozoa.
This invention aims to solve the aforementioned global health, hygiene and environment pandemic by providing a cost effective method for hygienic disposal of human, animal and bird excreta (and/or bio hazard).
SUMMARY OF INVENTION
The present invention relates to a formulation that absorbs and converts human, animal and bird excreta (and/or bio hazard) into a fragrant and upto 99.99% germ free gel or granules which may be either bio-degradable or non-biodegradable.
Formulation comprises of organic and/or inorganic chemical ingredients but not limited to absorbent ingredients, biocide, binding element combined with fragrance additive, anthelmintic, anti-protozoals that may further be combined with specially formulated safe bacterial culture that have the ability to degrade excreta or bio hazards into simpler bio-degradable compounds.
The process for preparation of formulation includes organic and inorganic ingredients; absorbent ingredient, biocides and fragrance additiveas primary components, optional organic and inorganic ingredients include but not limited to binder, anthelmintic, antiprotozoal, specially formulated safe bacterial culture, and urea.
DETAILED DESCRIPTION OF INVENTION
To restate, the present invention relates to a unique formulation useful in hygienic disposal of human and animals including bird excreta and/or biohazard into a fragrant and up to 99.99% germ free biodegradable and/or non-biodegradable gel or granules. The formulation includes absorbent ingredient, biocide, binding element, fragrance additive, bacterial culture anthelmintic, anti-protozoal, urea and other additives providing an easy and safe way to kill or inactivate the microorganisms.
There are various definitions enclosed herein, such as excreta is defined as waste matter discharged from the body of humans, animals and birds such as but not limited to urine, feces, vomit, spit, saliva.
Biohazards are defined as any biological or chemical substance that is dangerous to humans, animals, or the environment. Biohazard is further defined as waste from humans, animals and birds which includes items such as but not limited to blood, body tissues, body fluids (semen, cerebrospinal fluid, pleural fluid, vaginal secretions, pericardial fluid, amniotic fluid, saliva, peritoneal fluid), body parts, microbiological wastes(specimen cultures, disposable culture dishes, discarded viruses, and devices used to transfer or mix cultures), Pathological waste (unfixed human tissue (excluding skin), waste biopsy materials, and anatomical parts from medical procedures or autopsies)
The term germ (pathogen) is defined as an infectious microorganism or agent that causes disease. Germs can be transmitted a few ways depending on the type. They can be spread through skin contact, bodily fluids, airborne particles, contact with feces, and touching a surface touched by an infected person. There are different types of germs such as viruses, bacteria, fungi and spores.
Living Environment is defined as any building or space, frequented or lived in by humans, animals and birds.
Natural environment is defined as nature and water bodies. This environment encompasses the interaction of all living species, climate, weather and natural resources that affect human survival and economic activity.
Bacterial culture is defined as engineered aerobic and non anaerobic bacteria that have the ability to break down/degrade excreta/biohazards into simple bio degradable compounds.
Surface is defined as a porous or non-porous surface such as but not limited to carpet, fabric, floors, grass, soil from where excreta, bio hazard, or any waste material is to be removed.
When introducing elements of the present disclosure or the embodiments thereof, the articles “a,” “an,” and “the” are intended to mean that there are one or more of the elements. Similarly, the adjective “another,” when used to introduce an element, is intended to mean one or more elements. The terms “including” and “having” are intended to be inclusive such that there may be additional elements other than the listed elements.
Preferably, in the novel formulation disclosed herein, absorbent ingredients 60- 98%, biocides 0.01% - 15%, fragrance additives 0.5% - 2.5%, binder 0 - 30%, anthelmintic0 - 3%, antiprotozoal 0 - 4%, urea 0 - 10% and/or specially formulated safe aerobic/anaerobic bacterial culture0% - 10%which have the ability to degrade human oranimal excreta into simpler bio degradable compounds.
In one embodiment, the absorbent ingredient contained in the formulations of the present invention is selected from but not limited to inorganic absorbent ingredients such as, sodium and potassium polyacrylates while organic absorbent ingredients such as bamboo fiber, wood pulp, air laid wood pulp, absorbent non woven paper/fabric (made of wood pulp, fiber).In one embodiment, the biocide contained in the formulations of the present invention is selected frombut not limited to quaternary compounds, phenolic compounds, chlorhexidine compounds, chlorine-releasing agents.
Few examples of quaternary compounds are but not limited to benzalkoniumchloride, dimethyl benzyl ammonium saccharinate, dimethylbenzyl ammonium chloride, dimethylethylbenzyl ammonium chloride, didecyl dimethyl ammonium chloride.Few examples of phenolic compounds are but not limited to O-benzyl-p-chlorophenol, chlorophenol, chloroxylenol, O-phenylphenol. Few examples of chlorhexidine compoundsare but not limited to chlorhexidinediacetate(CHA), chlorhexidinedihydrochloride, chlorhexidinedigluconate, chlorhexidinegluconate, chlorhexidinephosphanilate. Few examples of chlorine-releasing agents are but not limited to sodium hypochlorite, glutardehyde, ortho-phthalaldehyde, peraceticacid, hydrogen peroxide/hydrogen peroxide silver, chlorine dioxide, potassium peroxymonosulfate, sodium chlorideandorganicbiocideasneem.
Various embodiments of the formulations using the abovementioned biocides have been tested and have shown confirmed “-cidal,-cide, -static” activity on over 150 types of germs;Bacteria, Virus, Fungi, Allergens, Yeasts as outlined below:
Bacteria can be but not limited to Mycobacterium tuberculosis, Mycobacterium bovis, Salmonella choleraesuis, Staphylococcusaureus, Pseudomonas aeruginosa, Pseudomonas cepacia, Pseudomonas maltophilia, Salmonellaarizonae, Salmonella enteritidis, Salmonella gallinarum, Salmonella pullorum, Salmonella sonnei, Salmonella paratyphi, Salmonella schottmuelleri, Salmonella typhi (Salmonella typhosa), Salmonella typhimurium, Shigelladysenteriae, Shigellaflexneri, Staphylococcus epidermis, Staphylococcus hyicus, Enterobacteraerogenes, Enterococcus sp., Enterococci group D sp., Enterococcus faecalis, Enterobacterchloacae, Escherichia coli, Proteus vulgaris, Proteusmirabilis, Klebsiellapneumoniae, Neisseria catarrhalis, Neiserriaelongata, Serratiamarcescens,Streptococcuspyogenes, Streptococcus salivarius, Streptococcus hemolyticus, Streptococcus equi, Streptococcus suis, Taylorellaequigenitalis, Diplococcuspneumoniae, Corynebacteriumdiptheriae, Providenciarettgeri, Alcaligenesfaecalis, Bordetellabronchiseptica, Mycoplasmasynoviae, Mycoplasma gallisepticum, Pasteurellaanatipestifer, Pasturellamultocida,Rhodococcusequi, Brevibacteriumammoniagenes, odor-causing bacteria, slime-forming bacteria, ammonia-producing bacteria. Clostridium difficile (C Difficile), Vibrio cholerae, Campylobacter jejuni, Listeria monocytogenes, Salmonella entericaAlcaligenes sp. ,Diplococcuspneumoniae Type 1, Lactobacillus delbrueckli subspecies lactis, Pasteurellamultocida, Shigellasonnei, Pseudomonas fluorescens (biotype B), Pseudomonas solanacearum, Pseudomonas cichorii, Erwiniacaratovora, Erwiniachrysantemi, Agrobacterium tumifaciens, Xanthomonascampestria, Aeromonashydrophila, Bordetellaavium, Corynebacteriumsepedonicum, Klebsiellapneumoniae, Salmonella enteritidis,Anitbiotic Resistant Bacteria:Staphylococcusaureus (MRSA) , Klebsiellapneumoniae - NDM-1 positive, Klebsiella pneumonias Carbapenem Resistant, Escherichia coli with extended beta-lactamase resistance (ESBL) , Multi-Drug Resistant (MDR) Acinetobacterbaumannii, Multi-Drug Resistant (MDR) Enterobacteraerogenes, Klebsiellapneumoniae with extended beta-lactamase resistance (ESBL), Penicillin Resistance Streptococcus pneumoniae (PRSP) , Klebsiellapneumoniae -NDM-1 positive.
Fungi can be but not limited to Tricodermaviride,Trichophytoninterdigitales, Trichophytonmentagrophytes, Trichophytonequinarum, Candida albicans, Microsporumcanis, Microsporumgypseum, Aspergillusniger, Aspergillusfumigatus, Pennicilliumglaucum, Verticilliumfungicola, Mycogoneperniciosa, Dactyliumdendroides, Botrytis cinerea, Phytophthoracinnamoni, Phthiumultimum, Rhizoctoniasolani, Verticilliumalboatrum.
Viruses can be but not limited to Human Immunodeficiency Virus Type 1 , Hepatitis B Virus, Hepatitis C Virus, H1N1 Influenza A Virus, Human Coronavirus SARS, Rhinovirus Type 39 (common cold) , Rotavirus WA (infectious diarrhea) Norovirus, Duck Hepatitis B Virus (DHBV) , Polio I virus, Rhinovirus, Feline Picornavirus, Avian Reovirus, Mouse Hepatitis virus, Vaccinia virus, Herpes simplex Type 1, Herpes simplex Type 2, Pseudorabies, avian infectious bronchitis, Avian Adenovirus, avian influenza, Avian Rotavirus, porcine transmissible gastroenteritis, Porcine Rotovirus, Influenza Type A/Mich, Influenza A /England, Influenza A (Japan, Asian, Hong Kong), Newcastle disease, mumps virus), Human Rhinovirus Type , Feline Leukemia virus, Rubella, equine arteritis, Avian Laryngotracheitis virus, Parainfluenza virus, Adenovirus Type 2, Canine Parvovirus, duck enteritis, Equine Herpes virus, Equine Rotavirus, Feline Calicivirus, Feline Rhinotracheitis. Avian influenza Virus, Avian Bronchitis Virus, Avian Laryngotracheitis Virus, Avian Herpes Virus 2, Hog Cholera Virus, Pseudorabies Virus, Influenza A , Herpes Simplex, Adenovirus Type 2 & 4 , Vaccinia Virus, Adenovirus Type 5, Herpes Simplex Type 2, Herpes simplex WI-38, Ebola Virus.
Yeasts can bebut not limited to Candida albicans, Saccharomyces cerevisiae.
Helminths are also known as parasitic worms which involves but not limited to the three major assemblages of parasitic helminthes such as Nemathelminthes (nematodes) , Platyhelminthes (flatworms) including its subdivisions Cestoda (tapeworms) and Trematoda (flukes).
Protozoal pathogens include but not limited to Entamoebahistolytica, Giardialambia, Balantidium coli, Cryptosporidium parvum, Cyclosporacayetanensis, Campylobacter, non-typhoidal Salmonella (NTS), Lassa virus, Cryptosporidium, Toxoplasma gondii.
In one embodiment, fragrance additives contained in the formulations of the present is selected from but not limited to natural fragrance additives (organic, chemical free) suchasorange, pomegranate, rosemary melon, watermelon, citrus, lemon, kiwi, lavender, cinnamon, dragon fruit. Furthermore, inorganic Fragrance Additives (chemical/industrial fragrances) include, apple, passion fruit, rose, citrus, orange, mango, wild berries, raspberry, peach, strawberry, waterlilly, watermelon, citrus, mogra.
In one embodiment, the binder additive contained in the formulations of the present invention may include but not limited to modified starch and aerosil.
In one embodiment anthelmintic contained in the formulations of the present invention is selected from but not limited to albendazole, fenbendazole, levamisole, oxyclozanide, tetramisole, iveremectin, praziquantel, ureaCO(NH2)2, peracetic acid.
In one embodiment bacterial culture contained in the formulation of the present invention is selected from specially formulated safe aerobic or anaerobic bacteria which have the ability to degrade human or animal excreta &bio hazard into simpler bio degradable compounds.
In preferred embodiment, there are various examples of formulations contained in the present invention includes sodiumsuper absorbent polyacrylate in the range of 60%-80% followed by addition of binder in the range of 0.1%– 40% with adding fragrance additive 0.05% to 1%.Furthermore, biocide in the range of 0.01% to 15% and anthelmintic in the range of 0.05% to 1.5% added to the formulation which may further combined with an additive to raise the pH level of the formulation which may include urea by weight in the range of 0.001 to 30%.
Further trials were performed on potassium super absorbent polyacry latein the range of 60%-80% followed by addition of binder in the range of 20%– 40% with adding fragrance additive 0.05% to 1%. Furthermore, Biocide in the range of 0.01% to 15% and anthelmintic in the range of peracetic acid 4% added to the formulation.
The formulations optionally comprise organic absorbent ingredient in the range of 70-90% with organic fragrance additive in the range of0.05% to 1% followed by addition of organic biocide in the range of 0.01% to 15%.
A formulation used for converting human and animal excreta and bio hazards wherein proportion of the organic and inorganic ingredients can be altered depending on the prevailing environment of the country, nature and type of excreta.
The process for preparation of formulation includes absorbent material and biocides as primary components to which optionally added are organic or inorganic ingredients not limited to binder, fragrance additive, antiprotozoal and/or specially formulated safe bacterial culture either by way of simple adding or spraying and mixing. In this process it is taken care that all primary components are properly mixed with additional ingredients.
In preferred embodiment, the present invention includes a process for conversion of excreta into a gel or granules, to achieve the aforementioned formulation is uniformly sprinkled to cover the entire surface area of the excreta at the rate of 1to 2.5 gm of formulation per 50 ml/gm of excreta. The formulation absorbs and converts the excreta into a gel or granules within 60 seconds. The time may increase depending upon the nature of excreta. After the conversion of the excreta into gel or granules, remove the gel or granulesfrom the surface by using a broom and dusting panand dispose as per local bio waste management laws. Here, the amount of formulation used for the conversion of excreta into a gel or granules specifically varies depending upon the nature of the excreta.
The product of present invention kills up to 99.9% germs in about 60seconds to 10 minutes. Hence, the product of present invention when used in any environmentwill provide containment of germs at source (in excreta and/or bio hazards), thereby stopping the transmission of germs from human and animal excreta. This will result in a healthier and safer environment for all beings and ultimately have a positive impact on mother nature.
The formulation may be deployed in various forms such as but not limited to powder, granules, sachets, water soluble sachets, discs, tablets, dissolvable paper which may be placed in various receptacles such as but not limited to paper , plastic, biodegradable or nonbiodegradable, steel, composite materials; bags, glass, cups, paper, bed pans, portable/fixed toilets, bottles.
EXAMPLES OF INVENTION
Formulations of the present invention are described in more detail with reference to the following examples. These examples are provided by way of illustration only and should not be construed as to limit the scope or spirit of the appended claims in any manner.
Table 1
Components* Example 1 Example 2 Example 3
Absorbent 75 % -90 % 90-99% 96 %
Biocide 0.01% - 7 % 0.8% - 3% 0.8% - 1%
Binder 20 % - 30 % 0% 1%
Fragrance additive 0.1 % - 2 % 0.5% - 5% 1-3%
Antihelminthic/Anti Protozoal ** 0.5 % - 2 % Nil Nil
Specially Formulated Bacterial culture 1% to 10% Nil Nil
* Here, components are in the percentage range.
** A urea as an additive may further be combined or replace the anthelmintic by weight of 0.1 % - 30% to raise the pH level of the formulation in order to deactivate the helminths and other parasites.
Formulations of the present invention as described herein are suitable for making or using in the industry.
A formulation used for converting human, animal or bird excreta and bio hazards wherein proportion of the organic and inorganic ingredients can be altered depending on; the prevailing environment of the country, nature and type of excreta.
Few methods of use of few for mulations of present invention are as mentioned below.
Method1: for disposal of feces including solid, semi solid bio hazards from all types of surfaces
Step 1: Sprinkle 1 to 2.5 grams of the formulation per 50 grams of feces to deodorize and disinfect the feces.
Step 2: remove the feces from the surface using commonly used methods for disposing it such as; scooping it with a bag, broom and dusting pan or poop picker.
Step 3: pour or spray 20-100 ml water onto the soiled surface and scrub it using any cleaning apparatus such as a broom or scrub to remove the feces residue (if any) from the surface.
Step 4: Sprinkle 1 to 2.5 grams of the formulation on the surface to cover the entire surface area of the spill (water) and wait for upto 60 seconds* for the formulation to absorb the water and residue on the surface.
*duration of time may increase based on the quantity and nature of feces and the quantity of formulation sprinkled onto the spill.
Step 5: remove the gel from the surface by using a method such as a broom/dusting pan, cleaning with a cloth or a vacuum cleaner which can vacuum liquid & solids.
Step 6: dispose as per local bio waste management laws.
Step 7: repeat step 2 to 6 if necessary.
Method 2: for conversion of liquid excreta into a gel or granules from all surfaces
Step 1: Sprinkle the formulation evenly to cover the entire surface area of the liquid excreta at the rate of 1-2.5 gram of formulation per 50 ml of liquid excreta.
Step 2: wait for up to 60* seconds for the powdered formulation to absorb and convert the liquid excreta into a gel or granules.
* duration of time taken to absorb and convert the liquid excreta may increase based on its nature/consistency.
Step 3: remove the gel or granules from the surface by using a method such as a broom/dusting pan, wiping with a cloth or a vacuum cleaner which can vacuum liquid and solids.
Step 4: dispose as per local bio waste management laws.
Step 5: repeat step 1 to 4 to remove any residual liquid excreta from the surface.
Laboratory test of examples of Table 1 is carried out for its antimicrobial activity. Powder form of present invention randomly selected for testing comprises absorbent, fragrance additive and biocides in which biocide comprises Alkyl Dimethyl Benzyl Ammonium Chloride and Alkyl Dimethyl Ethyl Benzyl Ammonium Chloride. The product evaluated for its antimicrobial activity in laboratory on pathogenic bacteria, fungi and sporocides which are major microorganism responsible for diseases to human or animal. which Table 2 shows bactericidal, fungicidal, and sporicidal activities of product.
Escherichia coli (E.coli) is Gram-negative straight rod bacteria, facultatively anaerobic chemoorganotroph capable of both respiratory and fermentative metabolism. Pathogenic E.coli strains are responsible for infection of the enteric, urinary, pulmonary and nervous systems. E.coli strains shows the core genome to be about 2000 genes while the pan-genome has over 18,000 genes. There are multiple, striking integration hotspots that are conserved across the genomes, corresponding to regions of abundant and parallel insertions and deletions of genetic material.Strain ATCC 8739 is a fecal strain. It is used to test the efficiency of antimicrobial agents. To test excreta in the present invention ATCC 8739 of E.Coli is selected.
Staphylococcus aureus sub spices aureus strain ATCC 6538 is a standard testing strain for disinfectants was initially isolated from a human lesion prior to the introduction of the widespread use of antimicrobials. This strain is selected for testing because it is important not only for routine screening in antimicrobial susceptibility testing but also for studying the evolution of resistance to biocides.
Bacillus subtilis (B. subtilis ) is a gram-positive, aerobic, spore-forming soil bacterium ubiquitous in the environment. In the literature, only a few cases of infections due to B. subtilis are reported and only one retrospective study describes the isolation of antibiotic-resistant strains of B. subtilis.
Fungal genus Candida causes a disease invasive candidiasis. It is a serious infection that can affect the blood, heart, brain, eyes, bones, and other tissues (Antinori et al., 2016). Moreover, it is the most common fungal disease among hospitalized, oncologic and immune suppressed patients in the developed world (Antinori et al., 2016). Mucosal infections are also very common, with vulvovaginal candidiasis (VVC) being the second most frequent gynecological condition after bacterial vaginosis (Anderson et al., 2004). VVC is a disease that significantly impacts the quality of life of affected women worldwide, particularly those with chronic and recurrent infections (Sobel, 2016). Out of many Candida multidrug-resistant Candida albicans has been selected for testing the product of present invention.
Testing is done using Dey-Engley neutralizing broth to neutralise the residual action of the disinfectants on the microbiological growth. Dey-Engley Neutralizing Broth is used in disinfectant testing where neutralization of the antiseptics and disinfectants is important for determining bactericidal activity. Bactericidal activity is measured by percentage log reduction of bacterial count.
Test Condition:
Amount of powder tested: 5gm
Biocides in the Composition: Alkyl Dimethyl Benzyl Ammonium Chloride 0.250%andAlkyl Dimethyl Ethyl Benzyl Ammonium Chloride 0.250%
Contact time: 60 seconds 2,5 and 10 Minutes
Incubation temperature: 34° C, 25°C
Neutralizer used: Dey engley neutralizing broth
Bactericidal, Fungicidal, and Sporocidal activity is shown in below table by along with initial count and % of age reduction at time interval of 1, 2, 5 and 10 minutes
Table 2
Organism Used Initial count Cfu/ml After 60 seconds After 2
minutes After
5 minutes After
10 minutes
Escherichia Coli (ATCC 8739) 82000000 62.19 87.80
99 .02
99.97
Staphylococcus aureus (ATCC 6538) 74000000 70.27 93.24
98 .78
99.95
B. Subtilis
(ATCC 6633) 65000000 56.92 89.23
95.38
99.96
Candida albicans (ATCC 10231) 5400000 59.25 83 .33 97 .77 99.90
The above result shows that after 60 seconds more than 55 – 70% any type of germs killed and in 2 – 10 minutes about 99.97% are killed. This proves that product of present provides containment of germs (pathogens and source) and thereby stopping the transmission or spreading of germs from any type of excreta of human and animal.
It should be understood that various changes and modifications to the various aspects/embodiments described herein will be apparent to those skilled in the art. Such changes and modifications can be made without departing from the spirit and scope of the subject matter of the present invention and without diminishing its intended advantages. It is therefore intended that such changes and modifications be covered within the scope of the present invention and claims.
Structures, substances, excipients, and methods that perform substantially the same function in such way to achieve substantially the same results are included within the scope of the claims.
,CLAIMS:
1. A formulation used for converting human and animal excreta and bio hazards into biodegradable or non bio-degradable up to 99.99% germ free, fragrant gelor granules for easy hygienic disposal.
2. A formulation used for converting human and animal excreta and bio hazards as claimed in claim 1, wherein the formulation comprises of organic and / or inorganic ingredients; absorbent, biocide, binder, fragrance additive, anthelmintic, anti protozoal and bacterial culture.
3. A formulation used for converting human and animal excreta and bio hazards as claimed in claim 1, wherein proportion of the organic and inorganic ingredients can be altered based on the prevailing environment of the country, nature and type of excreta.
4. A formulation used for converting human and animal excreta and bio hazards as claimed in claim 1, wherein formulation can be deployed in various forms such as powder, granules, sachets, discs, tablets, dissolvable paper that may be placed in various receptacles made up of paper, plastic, steel or composite materials.
5. A formulation used for converting human and animal excreta and bio hazards as claimed in claim 1, wherein the biodegradability or non-biodegradability of the formulation depends upon the composition and nature of ingredients.
6. A formulation used for converting human and animal excreta and bio hazards as claimed in claim 1, wherein formulation comprises:
absorbent about 60 - 98%;
biocides about 0.01% - 15%;
fragrance additives about 0.5% - 2.5%.
7. A formulation used for converting human and animal excreta and bio hazards as claimed in claim 1, wherein formulation comprises up to about 30% of binder.
8. A formulation used for converting human and animal excreta and bio hazards as claimed in claim 1, wherein formulation comprises up to about 10% of anthelmintic, antiprotozoal and/or specially formulated safe bacterial culture
9. A method of deploying a formulation for converting human and animal excreta and biohazards into biodegradable or non-biodegradable up to 99.99% germ free, fragrant gel or granules, the method comprising the steps of:
spraying and/or impregnating the formulation of claim 1 on a substrate; and allowing the substrate to dry.
| # | Name | Date |
|---|---|---|
| 1 | 202011003449-PROVISIONAL SPECIFICATION [25-01-2020(online)].pdf | 2020-01-25 |
| 2 | 202011003449-POWER OF AUTHORITY [25-01-2020(online)].pdf | 2020-01-25 |
| 3 | 202011003449-FORM 1 [25-01-2020(online)].pdf | 2020-01-25 |
| 4 | 202011003449-COMPLETE SPECIFICATION [29-07-2020(online)].pdf | 2020-07-29 |
| 5 | 202011003449-Covering Letter [02-09-2020(online)].pdf | 2020-09-02 |
| 6 | 202011003449-Correspondence-Letter [03-09-2020(online)].pdf | 2020-09-03 |
| 7 | 202011003449-FORM-9 [18-10-2020(online)].pdf | 2020-10-18 |
| 8 | 202011003449-FORM 18A [23-10-2020(online)].pdf | 2020-10-23 |
| 9 | 202011003449-Request Letter-Correspondence [03-11-2020(online)].pdf | 2020-11-03 |
| 10 | 202011003449-Power of Attorney [03-11-2020(online)].pdf | 2020-11-03 |
| 11 | 202011003449-Form 1 (Submitted on date of filing) [03-11-2020(online)].pdf | 2020-11-03 |
| 12 | 202011003449-Covering Letter [03-11-2020(online)].pdf | 2020-11-03 |
| 13 | 202011003449-CERTIFIED COPIES TRANSMISSION TO IB [03-11-2020(online)].pdf | 2020-11-03 |
| 14 | 202011003449-Power of Authority [30-01-2021(online)].pdf | 2021-01-30 |
| 15 | 202011003449-Power of Authority [30-01-2021(online)]-1.pdf | 2021-01-30 |
| 16 | 202011003449-PETITION u-r 6(6) [30-01-2021(online)].pdf | 2021-01-30 |
| 17 | 202011003449-PETITION u-r 6(6) [30-01-2021(online)]-1.pdf | 2021-01-30 |
| 18 | 202011003449-OTHERS [30-01-2021(online)].pdf | 2021-01-30 |
| 19 | 202011003449-Information under section 8(2) [30-01-2021(online)].pdf | 2021-01-30 |
| 20 | 202011003449-FER_SER_REPLY [30-01-2021(online)].pdf | 2021-01-30 |
| 21 | 202011003449-Covering Letter [30-01-2021(online)].pdf | 2021-01-30 |
| 22 | 202011003449-Covering Letter [30-01-2021(online)]-1.pdf | 2021-01-30 |
| 23 | 202011003449-CLAIMS [30-01-2021(online)].pdf | 2021-01-30 |
| 24 | 202011003449-ENDORSEMENT BY INVENTORS [08-02-2021(online)].pdf | 2021-02-08 |
| 25 | 202011003449-FER.pdf | 2021-10-18 |
| 26 | 202011003449-US(14)-HearingNotice-(HearingDate-09-12-2021).pdf | 2021-11-24 |
| 27 | 202011003449-Correspondence to notify the Controller [06-12-2021(online)].pdf | 2021-12-06 |
| 28 | 202011003449-Written submissions and relevant documents [22-12-2021(online)].pdf | 2021-12-22 |
| 29 | 202011003449-RELEVANT DOCUMENTS [22-12-2021(online)].pdf | 2021-12-22 |
| 30 | 202011003449-RELEVANT DOCUMENTS [22-12-2021(online)]-1.pdf | 2021-12-22 |
| 31 | 202011003449-PETITION UNDER RULE 137 [22-12-2021(online)].pdf | 2021-12-22 |
| 32 | 202011003449-PETITION UNDER RULE 137 [22-12-2021(online)]-1.pdf | 2021-12-22 |
| 33 | 202011003449-Annexure [22-12-2021(online)].pdf | 2021-12-22 |
| 34 | 202011003449-PatentCertificate30-12-2021.pdf | 2021-12-30 |
| 35 | 202011003449-IntimationOfGrant30-12-2021.pdf | 2021-12-30 |
| 36 | 202011003449-RELEVANT DOCUMENTS [08-09-2022(online)].pdf | 2022-09-08 |
| 1 | 2020-10-1622-25-02E_11-11-2020.pdf |