Product Description
| products appearance |
Light yellow, flat surface, no cracks, no visible impurities and bubbles |
| physicochemical property |
PH acceptable, gel strength 500-750g/cm2 |
| Sterility and water retention |
30-35ºC,Culture for 5 days, no bacterial growth,Culture for 5 days, no bacterial growth, no obvious water loss phenomenon |
| Packing |
Class A laminar flow production line automatic canning, to avoid the risk of personnel pollution |
| Growth experiment |
Inoculate the corresponding strains 50-100CFU according to the pharmacopoeia, and the ratio of the mean number of colonies on the test solid medium to the mean number of colonies on the control medium should be within the range of 0.5-2, and the size of the colonies should be consistent with the colonies on the control medium |
Product Parameters
| Item |
Model |
description |
culture |
usage |
| CP020028 |
D55A |
PETRI DISH |
TSA |
Surface microbial sampling without disinfectant and antibiotic residues |
| CP020029 |
D55B |
PETRI DISH |
TSA with Lecithin and Tween 80 |
Surface microbial sampling of residual disinfectant |
| CP020030 |
D55C |
PETRI DISH |
TSA with Lecithin and Tween 80,Penicillin G |
Sampling of surface microorganisms from residual penicillin antibiotics |
| CP020032 |
D55E |
PETRI DISH |
SDA |
For fungal detection on surfaces |
| CP020033 |
D90A |
PETRI DISH |
TSA |
Microbial detection of airborne settling bacteria and floating bacteria without disinfectant and antibiotic residues |
| CP020034 |
D90B |
PETRI DISH |
TSA with Lecithin and Tween 80 |
Microbial detection of airborne settling bacteria and floating bacteria in residual disinfectants |
| CP020035 |
D90C |
PETRI DISH |
TSA with Lecithin and Tween 80,Penicillin G |
Microbial detection of airborne settling bacteria and floating bacteria with residual penicillin antibiotics |
| CP020037 |
D90E |
PETRI DISH |
SDA |
For airborne fungal detection |
| CP020075 |
D90F |
PETRI DISH |
TSA with Cephalosporinase |
Microbial detection of airborne sedimentation bacteria and floating bacteria with residual cephalosporin antibiotics |
| CP020109 |
D90G |
PETRI DISH |
EMB |
Isolation and identification of Escherichia coli and Aerogenes |
| CP020110 |
D90H |
PETRI DISH |
NA |
Generally used for bacterial culture, transfer, rejuvenation, bacterial enhancement |
| CP020116 |
D90R |
PETRI DISH |
R2A |
For the determination of the total number of colonies in purified water |
Our collection incubator is the result of meticulous craftsmanship, embodying excellence through forty precise manufacturing processes. Each stage adheres strictly to the ISO9001 quality system and ISO14001 environmental standards, ensuring superior quality and sustainability. Every single product triumphantly passes the integrity test, a testament to our unwavering commitment to quality enhancement and traceability. We cater to diverse testing requirements across varying dosage forms and packaging, by selecting the finest cups, filter materials, and complementary needles. As a result, we've ingeniously designed and developed a range of collection incubators to impeccably satisfy the needs of various sterilization tests.
Sterility Testing for Product Rinse Solutions
Integrated Product Offering: The product rinse sterility test is meticulously tailored for products featuring hollow tubes, such as infusion and transfusion sets. These are products unsuitable for soaking, where the fluid channel is distinctly marked as sterile. This method, noted for its simplicity, necessitates the adaptation of FTM media with liquid D for rinse products. Following this, the eluate undergoes membrane filtration and is placed in both FTM and SCDM. Despite its efficiency, this method sees limited use in practice.
Bulk Pharmaceuticals and Biopharmaceuticals
Bulk pharmaceuticals (Active Pharmaceutical Ingredients - API) are thoroughly sterilized in strict accordance with USP 71 protocols before they are released into the manufacturing process.
Bulk biopharmaceuticals undergo rigorous sterility testing as mandated by 21 CFR 610.12. This involves the use of a medium (FTM) and specified sample test sizes as detailed in the regulations, ensuring a minimum capacity of not less than 10 ml.
Understanding Sterility Test Outcomes
Technicians are required to undergo comprehensive training in growth testing methods during the cultivation process. Growth is identified by examining a medium usually clear with respect to light, where a turbid area signals microbial presence. Upon detecting growth, the suspect container undergoes thorough testing to confirm that turbidity stems from microbial activity, rather than sample decomposition. Occasionally, cloudiness may arise from particle shedding or chemical reactions with the medium. Post-testing, the sample returns to the incubator for the remainder of its incubation period. Samples exhibiting turbidity in the medium are transferred and showcased on the 14th day of the test, over a four-day display period.
Tags:
Innovative Laboratory Petri Dish
Cell Culture Dish Available for Bulk Purchase
Comprehensive Range of Petri Dish Products
Durable and Versatile Plastic Petri Dish
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