Pure Global AI
EUDAMED registration 00841709116964Yes

Midmark 630 HumanForm Procedure Chair

Midmark CorporationClass IEU EUDAMEDTrade name: Midmark
VerifiedEUDAMED · official EU database
Device classification
Risk class
Class I
CND nomenclatures code
V0880
Trade name
Midmark
Implantable
No
Reusable
No
Measuring function
No
Registration information
Primary DI
00841709116964
Basic UDI
00841709118692GT
Version date
March 02, 2022
Manufacturer last update
May 16, 2022
Active status
Yes
Manufacturer
Manufacturer name
Midmark Corporation
Country
United States
Country type
NON_EU
Address
60 Vista Drive Versailles
Email
ecampbell@midmark.com
Authorized representative
Name
CEpartner4U
SRN
NL-AR-000000111
Country
Netherlands
Address
13 Esdoornlaan Maarn
Email
office@cepartner4u.com
Telephone
+31343442524
Regulatory information
Competent authority
Ministerie van Volksgezondheid, Welzijn en Sport
Applicable legislation
MDR (REGULATION (EU) 2017/745 on medical devices)
Placed on the market
Netherlands
Market available
Belgium:2020-05-26~None, Denmark:2020-05-26~None, Finland:2020-05-26~None, France:2020-05-26~None, Germany:2020-05-26~None, Netherlands:2020-05-26~None, Norway:2020-05-26~None, Poland:2020-05-26~None, Spain:2020-05-26~None, Sweden:2020-05-26~None, Turkey:2020-05-26~None, United Kingdom (Northern Ireland only):2020-05-26~None
Device characteristics
Human tissues
No
Animal tissues
No
Device description (EMDN)

MEDICAL SUPPORT EQUIPMENT - ACCESSORIES

About this record

Access comprehensive regulatory information for Midmark 630 HumanForm Procedure Chair in the European Union medical device market through Pure Global AI's free database. This Class I device is registered with EU EUDAMED under Primary DI 00841709116964 and manufactured by Midmark Corporation in United States.

This page provides complete registration details including trade name (Midmark), manufacturer information, authorized representative details, competent authority (Ministerie van Volksgezondheid, Welzijn en Sport), and regulatory compliance data from the official EU EUDAMED medical device database. Pure Global AI offers free access to the European Union's complete medical device registry, helping global MedTech companies navigate EU MDR regulations efficiently.