CHESAPEAKE® Stabilization System 3608-90007
by VB Spine LLC
Ref 3608-90007Model 08858250000106R4
CHESAPEAKE® Stabilization System 3608-90007 is a Class I device made by VB Spine LLC, registered in EUDAMED on 31 Oct 2026 (Basic UDI-DI 08858250000106R4) and listed in FDA GUDID since 6 Apr 2021 (UDI-DI 10888857157644), 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 | Number08858250000106R4 10888857157644 | Date31 Oct 2026 | StatusActive |
| United States | GUDID listing GUDID | Number10888857157644 | Date6 Apr 2021 | StatusListed |
Official records
- EUDAMED public site 08858250000106R4
- AccessGUDID record 10888857157644
Across registries
- EUDAMED Basic UDI-DI 08858250000106R4 registered 31 Oct 2026 Active
- FDA GUDID UDI-DI 10888857157644 listed 6 Apr 2021 Listed
Timeline
- Listed FDA GUDID 10888857157644
- Registered EUDAMED 08858250000106R4
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- CHESAPEAKE® Stabilization System
- Generic name
- Surgical instrument handle, non-torque-limiting
- Device name
- Chesapeake Handle
- Model / Ref / Catalog
- 3608-90007, 08858250000106R4
- Primary DI / UDI-DI
- 10888857157644
- Basic UDI-DI
- 08858250000106R4
- Direct marketing DI
- 10888857157644
- FDA product code
- LXH
- EMDN code
- L091199 Orthopaedic prosthetics instruments, reusable - other
- GMDN term
- Surgical instrument handle, non-torque-limiting
- Device class
- Class I
- Regulation number
- 888.4540
- EU registration type
- Standard device
- EU market of registration
- Netherlands
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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