FDA device listing
220266MIL,220316,220342,220343,220344,220404,220405,220451,220462,220463,220466,220471,220471NR,220472,220472NR,220473,2…
FDA device listing 2038291030 · Avanos Medical, Inc.
Key facts
| Proprietary names | 220266MIL,220316,220342,220343,220344,220404,220405,220451,220462,220463,220466,220471,220471NR,220472,220472NR,220473,220473NR,220477,220481ANR,220481AUS,220481NZ,220481ZNR,220489NR,220490NR,220491NR,220493,220507,220507NR,220508,220508NR,220509,220509NR,220513,220513NR,220528,220532,220537,220539,220541,220542,220560,220561,220562,220563,220568,220573,220574,220575,220576,220577 |
|---|---|
| Owner/operator | Avanos Medical, Inc. |
| Owner/operator number | 2022573 |
| Product codes | OFQ |
| Device names | OFQ - Anesthesia Kit |
| Device class | Class II |
| Classification regulations (21 CFR) | 868.5120 |
| Review panels | Anesthesiology |
| Registered establishments | Avanos Medical, Inc., Avent S. de R.L. de C.V. |
| Establishment registrations | 9680425, 3011270181 |
| FEI numbers | 3007596547, 3011270181 |
| Establishment operations | Complaint File Establishment, Specification Developer, Manufacturer, Repackager/Relabeler |
| 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