FDA device listing
Newclip11561 (MS) - BIT, DRILL
FDA device listing 1866654363 · STERIS Corporation
Key facts
| Proprietary names | Newclip11561 (MS) - BIT, DRILL |
|---|---|
| Owner/operator | STERIS Corporation |
| Owner/operator number | 10042227 |
| Product codes | HTW |
| Device names | HTW - Bit, Drill |
| Device class | Class I |
| Classification regulations (21 CFR) | 888.4540 |
| Review panels | Orthopedic |
| Registered establishments | STERIS Schweiz AG, Synergy Health Allershausen GmbH, Synergy Health Ede BV, Synergy Health Ireland Ltd, Synergy Health Marseille SAS, Synergy Health Sterilisation UK Ltd, Synergy Health Westport Ltd |
| Establishment registrations | 8043792, 3002807310, 3002807314, 3009756327, 3010160527, 3010162973, 3010173425 |
| FEI numbers | 3002807036, 3002807038, 3002807040, 3002807041, 3002807310, 3002807314, 3002808269 |
| 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