Pad 40096500
by Maquet, Inc.
Ref 40096500
Pad 40096500 is a Class I device made by Maquet, Inc., registered in EUDAMED on 30 Oct 2026 (Basic UDI-DI 40467680136ABR) and listed in FDA GUDID since 22 Sep 2022 (UDI-DI 04046768028234), active as of 7 Nov 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 | Number40467680136ABR 04046768028234 | Date30 Oct 2026 | StatusActive |
| United States | GUDID listing GUDID | Number04046768028234 | Date22 Sep 2022 | StatusListed |
Official records
- EUDAMED public site 40467680136ABR
- AccessGUDID record 04046768028234
Across registries
- EUDAMED Basic UDI-DI 40467680136ABR registered 30 Oct 2026 Active
- FDA GUDID UDI-DI 04046768028234 listed 22 Sep 2022 Listed
Timeline
- Listed FDA GUDID 04046768028234
- Registered EUDAMED 40467680136ABR
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Pad
- Generic name
- Operating table mattress, basic
- Device name
- Cushion phased out
- Model / reference
- 40096500
- Primary DI / UDI-DI
- 04046768028234
- Basic UDI-DI
- 40467680136ABR
- FDA product code
- BWN
- EMDN code
- V080504 Patient transfer boards and tables
- GMDN term
- Operating table mattress, basic
- Device class
- Class I
- Regulation number
- 878.4950
- EU registration type
- Standard device
- EU market of registration
- Germany
- GUDID distribution status
- In Commercial Distribution
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