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Contour-Flex Valve and Shunt System CFRH

by Integra Neurosciences Implant (France) 2 variants

Listed FDA GUDID listing, not in commercial distribution

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10381780036784 UDI-DI Date1 Oct 2015ListedStatusListed GUDID: not in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Contour-Flex Valve and Shunt System
Generic Name
Ventriculo-peritoneal/atrial shunt
Model / Ref / Catalog
CFRH
Primary DI / UDI-DI
10381780036784
FDA Product Code
JXG
GMDN Term
Ventriculo-peritoneal/atrial shunt
Device Class
Class II
Regulation Number
882.5550
GUDID distribution status
Not in Commercial Distribution
MRI Safety
MR Safe

Properties

  • Sterile
  • Single Use
  • Implantable
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (7)

  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No