Makevale, Ltd.
Active in EUDAMEDUnited Kingdomfrom SRN EUDAMED FDA SRN GB-MF-000023376 FEI 1000356102
- Devices
- 3
- Registrations
- EUDAMEDFDA
- FDA recalls
- 0
At a glance
Market reach
- European Union
- EUDAMED actor
- United States
- FDA FEI
Catalogue
HC Powder Clear/1 250g Ref 85001/0.25
CE MDD EUDAMEDH C Universal pk Vein FR/29 1kg/500ml Ref 85029/UP
CE MDD EUDAMEDR.R.Lab Pk Vein FR/39 1kg/500ml Ref 87039/LP
CE MDD EUDAMED
Company details
- EUDAMED SRN
- GB-MF-000023376
- FDA FEI number
- 1000356102
- EU VAT number
- GB798603477
- EUDAMED status
- Active
- EUDAMED registered name
- Makevale Ltd.
- Registered address
- Valley House, Marsh Lane, SG12 9QP, Hertfordshire, United Kingdom (ex Northern Ireland)
- Website
- www.makevale.com
- [email protected]
- Phone
- +44 1920 460641
- PRRC contact
- Alpa Ahir
Frequently asked questions
How many devices does MAKEVALE, LTD. have in the registry?
The registry currently lists 3 devices for MAKEVALE, LTD.. Devices recorded under merged duplicate company entries are counted once.
Which registries list MAKEVALE, LTD.'s devices?
Among its 3 most recently registered devices, MAKEVALE, LTD. has devices listed in EUDAMED (3 devices).
What risk classes do MAKEVALE, LTD.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for MAKEVALE, LTD.'s devices are Class IIa. Each device page shows its own class and authorisation.
What are the newest devices from MAKEVALE, LTD. in the registry?
The most recently registered devices listed for MAKEVALE, LTD. include HC Powder Clear/1 250g, H C Universal pk Vein FR/29 1kg/500ml and R.R.Lab Pk Vein FR/39 1kg/500ml.