FineMEC Co., Ltd
Active in EUDAMEDSouth Koreafrom SRN EUDAMED FDA SRN KR-MF-000025542 FEI 3012440264
- Devices
- 4
- Registrations
- EUDAMEDFDA
- FDA recalls
- 0
At a glance
Market reach
- European Union
- EUDAMED actor
- United States
- FDA FEI
- Authorised rep.
- MDSS GmbHDE
Catalogue
Noblex Long Pulse Alexandrite Laser Ref K143666
Regimes: CE MDD 510(k) Registry: EUDAMED510(k)GUDID- Regimes: CE MDD 510(k) Registry: 510(k)
Nobleen Ref Nobleen-00
Regimes: CE MDD Registry: EUDAMEDGUDIDAileen Plus Ref Aileen Plus-00
Regimes: CE MDD Registry: EUDAMED
Company details
- EUDAMED SRN
- KR-MF-000025542
- FDA FEI number
- 3012440264
- DUNS number
- 688275345
- EU VAT number
- 110-81-76150
- EUDAMED status
- Active
- EUDAMED registered name
- FineMEC Co., Ltd
- Registered address
- 217, Heojun-ro, 07531, Seoul, South Korea
- Website
- www.finemec.net/
- [email protected]
- PRRC contact
- GiBaek Song
Frequently asked questions
How many devices does FineMEC Co., Ltd have in the registry?
The registry currently lists 4 devices for FineMEC Co., Ltd. Devices recorded under merged duplicate company entries are counted once.
Which registries list FineMEC Co., Ltd's devices?
Among its 4 most recently registered devices, FineMEC Co., Ltd has devices listed in EUDAMED (3 devices), FDA 510(k) (2 devices) and FDA GUDID (2 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do FineMEC Co., Ltd's devices fall under?
Among its 4 most recently registered devices, the classes recorded for FineMEC Co., Ltd's devices are Class IIb and Class II. Each device page shows its own class and authorisation.
What are the newest devices from FineMEC Co., Ltd in the registry?
The most recently registered devices listed for FineMEC Co., Ltd include Noblex Long Pulse Alexandrite Laser, Nobleen Long Pulsed Alexandrite & Nd: YAG Laser System, Nobleen and Aileen Plus.