6700-313-600
Ref 6700-313-600Model 08858250000665SD
6700-313-600 is a device classified as Class IIa in the EU and Class II in the US made by Stryker Corp., registered in EUDAMED on 3 Jun 2026 (Basic UDI-DI 08858250000665SD) and listed in FDA GUDID since 3 Jan 2017 (UDI-DI 07613327303865), active as of 23 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 | Number08858250000665SD 07613327303865 | Date3 Jun 2026 | StatusActive |
| United States | GUDID listing GUDID | Number07613327303865 | Date3 Jan 2017 | StatusListed |
Official records
- EUDAMED public site 08858250000665SD
- AccessGUDID record 07613327303865
Across registries
- EUDAMED Basic UDI-DI 08858250000665SD registered 3 Jun 2026 Active
- FDA GUDID UDI-DI 07613327303865 listed 3 Jan 2017 Listed
Timeline
- Listed FDA GUDID 07613327303865
- Registered EUDAMED 08858250000665SD
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Generic name
- Surgical irrigation/aspiration pump, reusable
- Device name
- Surgical Irrigation Pump
- Model / Ref / Catalog
- 6700-313-600, 08858250000665SD
- Primary DI / UDI-DI
- 07613327303865
- Basic UDI-DI
- 08858250000665SD
- Direct marketing DI
- 07613327303865
- FDA product code
- GEI
- EMDN code
- L1899 Electrosurgery instruments, reusable - other
- GMDN term
- Surgical irrigation/aspiration pump, reusable
- Device class
- Class IIa EUDAMEDClass II GUDID
- Regulation number
- 878.4400
- EU registration type
- Standard device
- EU market of registration
- Netherlands
- GUDID distribution status
- In Commercial Distribution
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Device class | Class IIa | Class II |
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