FDA device listing
Nose clip pad single patient use 892121,Nose clip reusable V-892895,Nose clip single patient use V-892900
FDA device listing 1244696279 · Jaeger Medical GmbH
Key facts
| Proprietary names | Nose clip pad single patient use 892121,Nose clip reusable V-892895,Nose clip single patient use V-892900 |
|---|---|
| Owner/operator | Jaeger Medical GmbH |
| Owner/operator number | 10092652 |
| Product codes | BXJ |
| Device names | BXJ - Clip, Nose |
| Device class | Class I |
| Classification regulations (21 CFR) | 868.6225 |
| Review panels | Anesthesiology |
| Registered establishments | Jaeger Medical America Inc., Jaeger Medical GmbH |
| Establishment registrations | 9615102, 3033959233 |
| FEI numbers | 1000271197, 3033959233 |
| Establishment operations | Complaint File Establishment, Repackager/Relabeler, Specification Developer |
| 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