FDA device listing
Snowden-Pencer Forceps (WM-FE,RR),V. Mueller Fistula Probe (ST-MF),V. Mueller Instrument Tip Protector (ST-MF),V…
FDA device listing 1929351580 · STERIS
Key facts
| Proprietary names | Snowden-Pencer Forceps (WM-FE,RR),V. Mueller Fistula Probe (ST-MF),V. Mueller Instrument Tip Protector (ST-MF),V. Mueller Needle Holder (ST-MF, WM-FE,RR) |
|---|---|
| Owner/operator | STERIS |
| Owner/operator number | 10091086 |
| Product codes | MDM |
| Device names | MDM - Instrument, Manual, Surgical, General Use |
| Device class | Class I |
| Classification regulations (21 CFR) | 878.4800 |
| Review panels | General & Plastic Surgery |
| Registered establishments | STERIS Corporation, STERIS Deutschland GmBh |
| Establishment registrations | 1923569, 3006554912 |
| FEI numbers | 1923569, 3006554912 |
| Establishment operations | Foreign Exporter, Repackager/Relabeler, 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