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Introcan Safety ® 2 4232000-02

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 Number04046955341672 UDI-DI Date25 Mar 2022ListedStatusListed 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  • Withdrawn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
Introcan Safety ® 2
Generic Name
Peripheral vascular intervention infusion catheter
Model / Ref / Catalog
4232000-02
Primary DI / UDI-DI
04046955341672
FDA Product Code
FOZ
GMDN Term
Peripheral vascular intervention infusion catheter
Device Class
Class II
Regulation Number
880.5200
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Conditional

Related devices

Category: Peripheral vascular intervention infusion catheter

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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