C.B.B. LIFELINE BIOTECH LIMITED
Cyprus Last updated 23 May 2026
- Devices
- 1
- Registries
- EUDAMED
- FDA recalls
- 0
Catalogue
LifeKit Ref LifeKit
What C.B.B. LIFELINE BIOTECH LIMITED makes
C.B.B. Lifeline Biotech Limited manufactures the LifeKit, a medical device designed for emergency cardiac resuscitation support. This product is intended to assist in the delivery of defibrillation therapy during out-of-hospital cardiac arrest events, helping to restore normal heart rhythm.
The company’s portfolio is classified under EU Medical Device Regulation (MDR) as Class IIb devices, indicating a moderate to high risk level. These devices are registered in the EU’s eudamed database, ensuring compliance with European Union regulatory requirements. The manufacturer is based in Cyprus.
Frequently asked questions
How many devices does C.B.B. LIFELINE BIOTECH LIMITED have in the registry?
The registry currently lists 1 device for C.B.B. LIFELINE BIOTECH LIMITED. Devices recorded under merged duplicate company entries are counted once.
Which registries list C.B.B. LIFELINE BIOTECH LIMITED's devices?
Among its 1 most recently registered device, C.B.B. LIFELINE BIOTECH LIMITED has devices listed in EUDAMED (1 device).
What risk classes do C.B.B. LIFELINE BIOTECH LIMITED's devices fall under?
Among its 1 most recently registered device, the classes recorded for C.B.B. LIFELINE BIOTECH LIMITED's devices are Class IIb. Each device page shows its own class and authorisation.
What are the newest devices from C.B.B. LIFELINE BIOTECH LIMITED in the registry?
The most recently registered devices listed for C.B.B. LIFELINE BIOTECH LIMITED include LifeKit.
Information
- Address
- 5, Propontidos street, Strovolos, Cyprus
- Website
- lifelinecordblood.com/
- [email protected]
- Phone
- +357 22817222
- EUDAMED SRN
- CY-PR-000048613