Sanquin Reagents B.V.
Active in EUDAMEDNetherlandsfrom SRN EUDAMED FDA SRN NL-MF-000000530 FEI 3014271897
- Devices
- 4
- Registrations
- EUDAMEDFDA
- FDA recalls
- 0
At a glance
Market reach
- European Union
- EUDAMED actor
- United States
- FDA FEI
Catalogue
Makropanel 16 Ref K1385
CE IVDD EUDAMEDAnti-Fyb AGT method Ref K1337
CE IVDD EUDAMEDPeliClass human IgG subclass Plus kit Ref M1895
CE IVDR CE IVDD EUDAMEDPeliControl Ref K1379
CE IVDD EUDAMED
Company details
- EUDAMED SRN
- NL-MF-000000530
- FDA FEI number
- 3014271897
- EU VAT number
- NL856862836B01
- EUDAMED status
- Active
- EUDAMED registered name
- Sanquin Reagents B.V.
- Registered address
- 125, Plesmanlaan, 1006 AD, Amsterdam, Netherlands
- Website
- www.essange-reagents.com/
- [email protected]
- Phone
- +31 20 4570707
- PRRC contact
- Nathalie Van der Meij
Frequently asked questions
How many devices does SANQUIN REAGENTS B.V. have in the registry?
The registry currently lists 4 devices for SANQUIN REAGENTS B.V.. Devices recorded under merged duplicate company entries are counted once.
Which registries list SANQUIN REAGENTS B.V.'s devices?
Among its 4 most recently registered devices, SANQUIN REAGENTS B.V. has devices listed in EUDAMED (4 devices).
What risk classes do SANQUIN REAGENTS B.V.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for SANQUIN REAGENTS B.V.'s devices are IVD general, IVD Annex II List A and IVD Annex II List B. Each device page shows its own class and authorisation.
What are the newest devices from SANQUIN REAGENTS B.V. in the registry?
The most recently registered devices listed for SANQUIN REAGENTS B.V. include Makropanel 16, Anti-Fyb AGT method, PeliClass human IgG subclass Plus kit and PeliControl.