KayserBetten GmbH & Co. KG
Active in EUDAMEDGermanyfrom SRN EUDAMED FDA SRN DE-MF-000006910 FEI 3006795806
- Devices
- 1
- Registrations
- EUDAMEDFDA
- FDA recalls
- 11 ongoing
At a glance
Market reach
- European Union
- EUDAMED actor
- United States
- FDA FEI, FDA recalls
Catalogue
KayserBett OLAF 135 Ref KB-OLAF135
Regimes: CE MDR Registry: EUDAMED
Company details
- EUDAMED SRN
- DE-MF-000006910
- FDA FEI number
- 3006795806
- EU VAT number
- DE 239519735
- EUDAMED status
- Active
- EUDAMED registered name
- KayserBetten GmbH & Co. KG
- EUDAMED abbreviated name
- KayserBetten
- Registered address
- 12, Rieper Str., 29683, Bad Fallingbostel, Germany
- Website
- www.kayserbetten.eu
- de-de.facebook.com/KayserBetten
- [email protected]
- Phone
- +49 5163 6595
- PRRC contact
- Jens Lübben
FDA recalls
Recalls initiated per year
- 2017 0
- 2018 0
- 2019 0
- 2020 0
- 2021 0
- 2022 0
- 2023 0
- 2024 0
- 2025 0
- 2026 1
2026
- 4 May 2026 Z-2212-2026 Class I Ongoing If the adjustment functions of the hand control, as instructed in the Manual, are not locked with the provided key when the patient (child) is unattended, there is an increased risk that the patient (child) or third parties (children) will operate the hand control and trap themselves or others under the bed frame or between the bed frame and the floor. This can lead to serious injuries or even death of the patient (child) or third parties (children).
From the company website
We at KayserBetten offer you child care beds that are perfectly adapted to your individual needs. Find out more!
Frequently asked questions
How many devices does KayserBetten GmbH & Co. KG have in the registry?
The registry currently lists 1 device for KayserBetten GmbH & Co. KG. Devices recorded under merged duplicate company entries are counted once.
Which registries list KayserBetten GmbH & Co. KG's devices?
Among its 1 most recently registered device, KayserBetten GmbH & Co. KG has devices listed in EUDAMED (1 device).
What risk classes do KayserBetten GmbH & Co. KG's devices fall under?
Among its 1 most recently registered device, the classes recorded for KayserBetten GmbH & Co. KG's devices are Class I. Each device page shows its own class and authorisation.
Are there FDA recall records for KayserBetten GmbH & Co. KG?
FDA recall records list 1 recall initiated by KayserBetten GmbH & Co. KG, the most recent initiated on 4 May 2026. 1 of them is recorded as ongoing. A recall is often a precaution started by the manufacturer; the records say nothing about the company's overall record.
What are the newest devices from KayserBetten GmbH & Co. KG in the registry?
The most recently registered devices listed for KayserBetten GmbH & Co. KG include KayserBett OLAF 135.