Crivel, S.a
Spainfrom SRN
- Devices
- 64
What Crivel, S.a makes
CRIVEL, S.A. manufactures vitreoretinal surgical instruments, including a 23-gauge vitrectomy probe designed for retinal procedures such as the H. Perpetuo Socorro Albacete Retina 23G. These tools are intended for use in ophthalmic surgeries, particularly for vitreous cavity management and retinal detachment repair.
The company’s portfolio is classified under EU Medical Device Regulation (MDR) as Class IIa devices and is registered in the EU’s eudamed database. CRIVEL, S.A. is based in Spain and adheres to EU regulatory requirements for medical device compliance.
Catalogue
Search and filter all 64 devicesShowing 1-50 of 64
Frequently asked questions
How many devices does CRIVEL, S.A have in the registry?
The registry currently lists 64 devices for CRIVEL, S.A. Devices recorded under merged duplicate company entries are counted once.
Which registries list CRIVEL, S.A's devices?
Among its 50 most recently registered devices, CRIVEL, S.A has devices listed in EUDAMED (50 devices).
What risk classes do CRIVEL, S.A's devices fall under?
Among its 50 most recently registered devices, the classes recorded for CRIVEL, S.A's devices are Class IIa. Each device page shows its own class and authorisation.
What are the newest devices from CRIVEL, S.A in the registry?
The most recently registered devices listed for CRIVEL, S.A include Pack Vitrectomía 23GH.U.Infanta Leonor(9311.23G01+424101/02), Pack Vitrectomia 23G H. G. Marañón(9311.23G01+423039/02), H. Perpetuo Socorro Albacete Combinada 25G(9310.25G02+426016/01) and Pack Comb.23G H.U.12 Octubre(9310.23G02+8430.18SF1+424074/02).