FDA device listing
RIM E.coli O157:H7 Latex
FDA device listing 1842342920 · Thermo Fisher Scientific
Key facts
| Proprietary names | RIM E.coli O157:H7 Latex |
|---|---|
| Owner/operator | Thermo Fisher Scientific |
| Owner/operator number | 2517925 |
| Premarket submissions | K933457 |
| Product codes | GNA |
| Device names | GNA - Antisera, All Types, Escherichia Coli |
| Device class | Class I |
| Classification regulations (21 CFR) | 866.3255 |
| Review panels | Microbiology |
| Registered establishments | REMEL EUROPE LTD, REMEL, INC. |
| Establishment registrations | 1924669, 3003750284 |
| FEI numbers | 1924669, 3003750284 |
| Establishment operations | Contract Manufacturer, Specification Developer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- 1–9 UDI devices (GUDID) under the same submission
- 1–9 Device listings citing the same submission
- Yes Premarket submission listed
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device listings
Establishments that make or process devices for the U.S. market must list each device with the FDA. A listing records the device's proprietary names, product codes and premarket submission, and every registered establishment that handles it.
Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database