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Midmark 9A556001

by Midmark Corporation

Ref 9A556001Model 630-010

Midmark 9A556001 is a Class I device made by Midmark Corporation, registered in EUDAMED on 14 Oct 2021 (Basic UDI-DI 00841709118692GT) and listed in FDA GUDID since 21 Oct 2020 (UDI-DI 00841709117978), active as of 22 Oct 2026.

Active European Union. Also listed in GUDID (US).

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number00841709118692GT Basic UDI-DI 00841709117978UDI-DIDate14 Oct 2021RegisteredStatusActive
United StatesGUDID listing GUDID Number00841709117978 UDI-DI Date21 Oct 2020ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 00841709118692GT registered 14 Oct 2021 Active
  • FDA GUDID UDI-DI 00841709117978 listed 21 Oct 2020 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00841709117978
  2. Registered EUDAMED 00841709118692GT

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade name
Midmark
Generic name
General examination/treatment chair, electric
Device name
Midmark 630 HumanForm Procedure Chair
Model / Ref / Catalog
9A556001, 630-010
Primary DI / UDI-DI
00841709117978
Basic UDI-DI
00841709118692GT
Direct marketing DI
00841709117978
FDA product code
GBB
EMDN code
V0880 Medical support equipment - accessories
GMDN term
General examination/treatment chair, electric
Device class
Class I
Regulation number
878.4960
EU registration type
Standard device
EU market of registration
Netherlands
GUDID distribution status
In Commercial Distribution

Similar devices in this category

Other devices filed under MEDICAL SUPPORT EQUIPMENT - ACCESSORIES.

Other devices from Midmark Corporation

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Properties

  • Premarket exempt
  • Serial number
  • Manufacturing date
Other properties (22, all answered No)