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CASCADIA™ Interbody System 6101-90045

by VB Spine LLC EUDAMEDGUDID

Active European Union

Ref 6101-90045Model 08858251004172SW

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number08858251004172SW Basic UDI-DIDate30 Aug 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number10888857269965 UDI-DIDate2 Sep 2016ListedStatusListed GUDID: in commercial distribution

Coverage

2 jurisdictions

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  • Withdrawn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

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.

Recalls

0 recalls · FDA

No FDA recalls on record, checked 24 Oct 2026.

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
6101-90045, 08858251004172SW
Primary DI / UDI-DI
10888857269965
Basic UDI-DI
08858251004172SW
Direct Marketing DI
10888857269965
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 — 18 degree
Height — 6 Millimeter
Width — 10 Millimeter
Length — 28 Millimeter

Truth per registry

2 sources · 2 fields differ

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

Other devices from VB Spine LLC

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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