FDA device listing
IDA II (KR13),IDA I (KR3),KayserBett Hannah135 (KR5),KayserBett Hannah170 (KR5),Olaf,,Timmy
FDA device listing 1574195281 · Kayserbetten GmbH & Co. KG
Key facts
| Proprietary names | IDA II (KR13),IDA I (KR3),KayserBett Hannah135 (KR5),KayserBett Hannah170 (KR5),Olaf,,Timmy |
|---|---|
| Owner/operator | Kayserbetten GmbH & Co. KG |
| Owner/operator number | 10023012 |
| Product codes | FNL |
| Device names | FNL - Bed, Ac-Powered Adjustable Hospital |
| Device class | Class II |
| Classification regulations (21 CFR) | 880.5100 |
| Review panels | General Hospital |
| Registered establishments | Kayserbetten GmbH & Co. KG |
| Establishment registrations | 3006795806 |
| FEI numbers | 3006795806 |
| Establishment operations | 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