FDA device listing
Biopsy Bags
FDA device listing 1337580797 · MERCEDES MEDICAL LLC
Key facts
| Proprietary names | Biopsy Bags |
|---|---|
| Owner/operator | MERCEDES MEDICAL LLC |
| Owner/operator number | 9033351 |
| Product codes | KET |
| Device names | KET - Filters, Cell Collection, Tissue Processing |
| Device class | Class I |
| Classification regulations (21 CFR) | 864.3010 |
| Review panels | Pathology |
| Registered establishments | MERCEDES MEDICAL LLC |
| Establishment registrations | 1063851 |
| FEI numbers | 1000442352 |
| Establishment operations | Complaint File Establishment |
| 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