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Actreen® 242210NA

by B. Braun Medical, Inc.

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04046955196623 UDI-DI Date3 Mar 2019ListedStatusListed 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  • Withdrawn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
Actreen®
Generic Name
Urine-sampling urethral catheter
Model / Ref / Catalog
242210NA
Description
Actreen® Hi-Lite Cath Straight Set 37cm 10 Fr
Primary DI / UDI-DI
04046955196623
FDA Product Code
GBM
GMDN Term
Urine-sampling urethral catheter
Device Class
Class II
Regulation Number
876.5130
GUDID distribution status
Not in Commercial Distribution
Size
Catheter Gauge — 10.0 French
Outer Diameter — 3.3 Millimeter
Length — 37 Centimeter

Other devices from B. Braun Medical, Inc.

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Properties

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

Other properties (9)

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