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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 European Union. Also listed in GUDID (US).

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, GUDID, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number08858250000106R4 Basic UDI-DI 10888857157644UDI-DIDate31 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number10888857157644 UDI-DI Date6 Apr 2021ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 08858250000106R4 registered 31 Oct 2026 Active
  • FDA GUDID UDI-DI 10888857157644 listed 6 Apr 2021 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 10888857157644
  2. Registered EUDAMED 08858250000106R4

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

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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Other devices filed under ORTHOPAEDIC PROSTHETICS INSTRUMENTS, REUSABLE - OTHER.

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Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (21, all answered No)