iFlash-Mycoplasma Pn. IgG
Catalogue number C88003G, listed by Shenzhen Yhlo Biotech Co., Ltd., China, under Antisera, All Mycoplasma Spp. 1 manufacturer in China is registered for this product code.
1manufacturer
1catalogue number
Who Else Makes It
Registered in Guangdong.
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| Shenzhen Yhlo Biotech Co., Ltd. | Shenzhen | Guangdong | Manufacturer | 19 |
Record
| Listed by | Shenzhen Yhlo Biotech Co., Ltd., China |
|---|---|
| FDA product code | GSA |
| Device type | Antisera, All Mycoplasma Spp. |
| Device class | Class 1 |
| Regulation | 21 CFR 866.3375 |
| Establishment | Manufacturer |
| Premarket notification | Exempt |
| Record published | 2022-10-26 |
Specifications
| MRI safety | Labeling does not contain MRI Safety Information |
|---|---|
| Label carries | lot or batch number, expiry date, manufacturing date |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| C88003G | In distribution |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| iFlash-Mycoplasma pn. IgM | Shenzhen Yhlo Biotech Co., Ltd. | 1 |
Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.