FDA device listing
De Bakey Forceps titanium, 195 mm length,De Bakey Forceps titanium, 240 mm length,Septal Hook, 3 prong, 10 mm hook…
FDA device listing 1555050532 · Berger Surgical Medical Products GmbH
Key facts
| Proprietary names | De Bakey Forceps titanium, 195 mm length,De Bakey Forceps titanium, 240 mm length,Septal Hook, 3 prong, 10 mm hook, angled up and ot the side,Septal Hook, 3 prong, 13 mm hook, angled up and ot the side,Septal Hook, 3 prong, 7mm hook, angled up and ot the side |
|---|---|
| Owner/operator | Berger Surgical Medical Products GmbH |
| Owner/operator number | 10055726 |
| Product codes | GEN |
| Device names | GEN - Forceps, General & Plastic Surgery |
| Device class | Class I |
| Classification regulations (21 CFR) | 878.4800 |
| Review panels | General & Plastic Surgery |
| Registered establishments | Berger Surgical Medical Products GmbH |
| Establishment registrations | 3013784566 |
| FEI numbers | 3013784566 |
| Establishment operations | Contract Manufacturer, 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