FDA device listing
BIOBLUE,BIOBLUE AMNIO,BIOBLUE DROP,BIOWHITE,BIOWHITE-AMNIO,BIOWHITE-SUPPLEMENT
FDA device listing 1956871509 · BIOVIEW LTD.
Key facts
| Proprietary names | BIOBLUE,BIOBLUE AMNIO,BIOBLUE DROP,BIOWHITE,BIOWHITE-AMNIO,BIOWHITE-SUPPLEMENT |
|---|---|
| Owner/operator | BIOVIEW LTD. |
| Owner/operator number | 9054795 |
| Product codes | PPM |
| Device names | PPM - General Purpose Reagent |
| Device class | Class I |
| Classification regulations (21 CFR) | 864.4010 |
| Review panels | Pathology |
| Registered establishments | BIOVIEW LTD. |
| Establishment registrations | 3003909093 |
| FEI numbers | 3003909093 |
| Establishment operations | Manufacturer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- None listed 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