FDA device listing
Drill, Bone, Powered
FDA device listing 1570068485 · Rose GmbH fuer Medizintechnik
Key facts
| Owner/operator | Rose GmbH fuer Medizintechnik |
|---|---|
| Owner/operator number | 10042910 |
| Product codes | DZI, ERL, HBC, HBE |
| Device names | DZI - Drill, Bone, Powered, ERL - Drill, Surgical, Ent (Electric Or Pneumatic) Including Handpiece, HBC - Motor, Drill, Electric, HBE - Drills, Burrs, Trephines & Accessories (Simple, Powered) |
| Device class | Class II |
| Classification regulations (21 CFR) | 872.4120, 874.4250, 882.4310, 882.4360 |
| Review panels | Dental, Ear, Nose, & Throat, Neurology |
| Registered establishments | ROSE GMBH FUER MEDIZINTECHNIK |
| Establishment registrations | 3002808022 |
| FEI numbers | 3002808022 |
| Establishment operations | Contract Sterilizer |
| 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