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CASCADIA™ Interbody System 6101-90189

by VB Spine LLC

Ref 6101-90189Model 08858251004172SW

Active European Union. Also listed in GUDID (US).

CE MDR

Valid until

Not listed

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

Registry data, not yet checked by deviCERTS. Source EUDAMED, GUDID, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number08858251004172SW Basic UDI-DIDate30 Aug 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number10888857290907 UDI-DIDate2 Sep 2016ListedStatusListed GUDID: in commercial distribution

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

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  • Withdrawn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
CASCADIA™ Interbody System
Generic Name
Spinal implant trial
Device Name
AN Lordotic Oblique Trials-Cascadia Interbody System
Model / Ref / Catalog
6101-90189, 08858251004172SW
Primary DI / UDI-DI
10888857290907
Basic UDI-DI
08858251004172SW
Direct Marketing DI
10888857290907
FDA Product Code
MAX
EMDN Code
L091199 Orthopaedic prosthetics instruments, reusable - other
GMDN Term
Spinal implant trial
Device Class
Class IIa EUDAMED
Class II GUDID
Regulation Number
888.3080
Market of Registration
Netherlands
GUDID distribution status
In Commercial Distribution
Size
Angle — 12 degree
Height — 10 Millimeter
Length — 32 Millimeter
Width — 10 Millimeter

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Device ClassEUDAMED
Class IIa
GUDID
Class II
SterileEUDAMED
No
GUDID
Yes

Related devices

Category: General internal orthopaedic fixation system implantation kit

Other devices from VB Spine LLC

See all devices from VB Spine LLC →

Properties

  • Sterile NoEUDAMEDYesGUDID
  • Prescription Use
  • Lot / Batch Number

Other properties (21)

  • Single Use: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Expiration Date: No
  • Manufacturing Date: No