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Clik-Fix® WCS-1000B

by B. Braun Medical, Inc.

Listed FDA GUDID listing, no authorization on record

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04046955803286 UDI-DI Date13 Mar 2023ListedStatusListed GUDID: 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  • Withdrawn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
Clik-Fix®
Generic Name
Wearable percutaneous catheter/tube holder, single-use
Model / Ref / Catalog
WCS-1000B
Primary DI / UDI-DI
04046955803286
FDA Product Code
KMK
GMDN Term
Wearable percutaneous catheter/tube holder, single-use
Device Class
Class I
Regulation Number
880.5210
GUDID distribution status
In Commercial Distribution

Related devices

Category: Wearable percutaneous catheter/tube holder

Other devices from B. Braun Medical, Inc.

See all devices from B. Braun Medical, Inc. →

Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date

Other properties (8)

  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No
  • Manufacturing Date: No