4200355040
Ref 4200-355-040Model 08858251002063SA
4200355040 (4200-355-040) is a device classified as Class IIa in the EU and Class I in the US made by Stryker Corp., registered in EUDAMED on 2 Oct 2026 (Basic UDI-DI 08858251002063SA) and listed in FDA GUDID since 23 Sep 2018 (UDI-DI 04546540217172), active as of 24 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 | Number08858251002063SA 04546540217172 | Date2 Oct 2026 | StatusActive |
| United States | GUDID listing GUDID | Number04546540217172 | Date23 Sep 2018 | StatusListed |
Official records
- EUDAMED public site 08858251002063SA
- AccessGUDID record 04546540217172
Across registries
- EUDAMED Basic UDI-DI 08858251002063SA registered 2 Oct 2026 Active
- FDA GUDID UDI-DI 04546540217172 listed 23 Sep 2018 Listed
Timeline
- Listed FDA GUDID 04546540217172
- Registered EUDAMED 08858251002063SA
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Generic name
- Surgical saw blade, sagittal, single-use
- Device name
- Radiolucent Drill Bits
- Model / Ref / Catalog
- 08858251002063SA, 4200-355-040, 4200355040
- Primary DI / UDI-DI
- 04546540217172
- Basic UDI-DI
- 08858251002063SA
- FDA product code
- GFG
- EMDN code
- V010302 Blades without safety systems, single-use - not included in other classes
- GMDN term
- Surgical saw blade, sagittal, single-use
- Device class
- Class IIa EUDAMEDClass I GUDID
- Regulation number
- 878.4820
- EU registration type
- Standard device
- EU market of registration
- Netherlands
- GUDID distribution status
- In Commercial Distribution
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Model / reference | 08858251002063SA 4200-355-040 | 4200355040 |
| Device class | Class IIa | Class I |
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