Midmark 9A684001-869
Part of a family of 197 devices: see the family page
Ref 9A684001-869Model 630-010
Midmark 9A684001-869 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 7 May 2020 (UDI-DI 00841709116933), active as of 22 Oct 2026.
Active
CE MDR
Valid until
No date given
FDA recalls
Not checked
Documents
None linked in EUDAMED
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR EUDAMED | Number00841709118692GT 00841709116933 | Date14 Oct 2021 | StatusActive |
| United States | GUDID listing GUDID | Number00841709116933 | Date7 May 2020 | StatusListed |
Official records
- EUDAMED public site 00841709118692GT
- AccessGUDID record 00841709116933
Across registries
- EUDAMED Basic UDI-DI 00841709118692GT registered 14 Oct 2021 Active
- FDA GUDID UDI-DI 00841709116933 listed 7 May 2020 Listed
Timeline
- Listed FDA GUDID 00841709116933
- Registered EUDAMED 00841709118692GT
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Midmark
- Generic name
- Operating/examination/treatment table headrest, reusable
- Device name
- Midmark 630 HumanForm Procedure Chair
- Model / Ref / Catalog
- 9A684001-869, 630-010
- Primary DI / UDI-DI
- 00841709116933
- Basic UDI-DI
- 00841709118692GT
- Direct marketing DI
- 00841709116933
- FDA product code
- GBB
- EMDN code
- V0880 Medical support equipment - accessories
- GMDN term
- Operating/examination/treatment table headrest, reusable
- Device class
- Class I
- Regulation number
- 878.4960
- EU registration type
- Standard device
- EU market of registration
- Netherlands
- GUDID distribution status
- In Commercial Distribution
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