Prolex E. Coli O157 Latex Reagent Control Negative
Negative Control Latex Reagent
3manufacturers in China registered for this device type
1catalogue number
1510(k) clearance
Who Else Makes It
All of them in Jilin.
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| Changchun Wancheng BIO-Electron Co., Ltd. | Changchun | Jilin | Contract manufacturer | 34 |
| Changchun Merydi BIO-Tech Co., Ltd. | Changchun | Jilin | Manufacturer | 24 |
| Jilin Hongyi BIO-Tech Co., Ltd. | Changchun | Jilin | Manufacturer | 24 |
Record
| Listed by | pro-lab incorporated, Canada |
|---|---|
| FDA product code | GNA |
| Device type | Antisera, All Types, Escherichia Coli |
| Device class | Class 1 |
| Regulation | 21 CFR 866.3255 |
| Establishment | Contract manufacturer, Manufacturer, Exporter |
| Premarket notification | Exempt |
| Record published | 2022-12-26 |
Specifications
| MRI safety | Labeling does not contain MRI Safety Information |
|---|---|
| Single use | Yes |
| Label carries | lot or batch number, expiry date |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| PL.076B | In distribution |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| Mast Assure Antisera | Mast Group Ltd. | 7 |
| E. coli O134 serum high titer, 1 mL | SSI Diagnostica A/S | 2 |
| Prolex E. coli O111 Latex Reagent | pro-lab incorporated | 1 |
| E. coli O73 serum high titer, 1 mL | SSI Diagnostica A/S | 1 |
| E. coli O25 serum, 1 mL | SSI Diagnostica A/S | 1 |
| E. coli O89 serum high titer, 1 mL | SSI Diagnostica A/S | 1 |
| ImmuLex E. coli O55, 1.5 mL | SSI Diagnostica A/S | 1 |
| E. coli O60 serum, 1 mL | SSI Diagnostica A/S | 1 |
| E. coli O10 serum high titer, 1 mL | SSI Diagnostica A/S | 1 |
| E. coli O110 serum, 1 mL | SSI Diagnostica A/S | 1 |
| E. coli O88 serum high titer, 1 mL | SSI Diagnostica A/S | 1 |
| E. coli O147 serum, 1 mL | SSI Diagnostica A/S | 1 |
Showing 12 of 492. All products under Antisera, All Types, Escherichia Coli
510(K) Clearances
| Clearance | Decision date |
|---|---|
| K903714 | 1991-01-24 |
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.