0682400606
by STRYKER Communications, Inc.
Ref 0682-400-606Model 08858250000752S9
0682400606 (0682-400-606) is a Class I device made by STRYKER Communications, Inc., registered in EUDAMED on 4 Nov 2026 (Basic UDI-DI 08858250000752S9) and listed in FDA GUDID since 29 Jul 2020 (UDI-DI 07613327054538), 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 | Number08858250000752S9 07613327054538 | Date4 Nov 2026 | StatusActive |
| United States | GUDID listing GUDID | Number07613327054538 | Date29 Jul 2020 | StatusListed |
Official records
- EUDAMED public site 08858250000752S9
- AccessGUDID record 07613327054538
Across registries
- EUDAMED Basic UDI-DI 08858250000752S9 registered 4 Nov 2026 Active
- FDA GUDID UDI-DI 07613327054538 listed 29 Jul 2020 Listed
Timeline
- Listed FDA GUDID 07613327054538
- Registered EUDAMED 08858250000752S9
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Generic name
- Medical monitor/light mount
- Device name
- COM_TF10468_Suspension
- Model / Ref / Catalog
- 08858250000752S9, 0682-400-606, 0682400606
- Primary DI / UDI-DI
- 07613327054538
- Basic UDI-DI
- 08858250000752S9
- Direct marketing DI
- 07613327054538
- FDA product code
- FQO
- EMDN code
- Z129099 Various instruments for functional exploration and therapeutic interventions - other
- GMDN term
- Medical monitor/light mount
- Device class
- Class I
- Regulation number
- 878.4960
- EU registration type
- Standard device
- EU market of registration
- Ireland
- GUDID distribution status
- In Commercial Distribution
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Model / reference | 08858250000752S9 0682-400-606 | 0682400606 |
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