FDA device listing
Air Injection Cannula 25GA angled at 5 mm,Air Injection Cannula 27GA angled at 5 mm,Air Injection Cannula 27GA angled at…
FDA device listing 1911532557 · Holger Bumueller LLC
Key facts
| Proprietary names | Air Injection Cannula 25GA angled at 5 mm,Air Injection Cannula 27GA angled at 5 mm,Air Injection Cannula 27GA angled at 7 mm,Air Injection Cannula, 27 Gauge, angled at 5mm 45 deg,Air Injection Cannula 30 GA angled at 5 mm,Air Injection Cannula 30 GA angled at 7 mm,Air Injection Cannula, 30 Gauge, angled at 5 mm 45 deg,Anis Aspir. Cannula 23 GA thin wall, angled,Anis Aspir. Cannula 23 GA thin… |
|---|---|
| Owner/operator | Holger Bumueller LLC |
| Owner/operator number | 10030046 |
| Product codes | HMX |
| Device names | HMX - Cannula, Ophthalmic |
| Device class | Class I |
| Classification regulations (21 CFR) | 886.4350 |
| Review panels | Ophthalmic |
| Registered establishments | HOLGER BUMUELLER LLC |
| Establishment registrations | 3007840839 |
| FEI numbers | 3007840839 |
| Establishment operations | Contract 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