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Magic3 Touchless™ Hydrophilic Intermittent Catheter System 58712

by C. R. Bard, 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 Number00801741104008 UDI-DI Date11 Jul 2016ListedStatusListed 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  • Withdrawn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
Magic3 Touchless™ Hydrophilic Intermittent Catheter System
Generic Name
Single-administration urethral drainage catheter
Model / Ref / Catalog
58712
Primary DI / UDI-DI
00801741104008
FDA Product Code
MJC
GMDN Term
Single-administration urethral drainage catheter
Device Class
Class II
Regulation Number
876.5130
GUDID distribution status
In Commercial Distribution
Size
Catheter Gauge — 12 French

Related devices

Category: Single-administration urethral drainage catheter

Other devices from C. R. Bard, Inc.

See all devices from C. R. Bard, Inc. →

Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Convenience Kit
  • Combination Product
  • Lot / Batch Number
  • Expiration Date

Other properties (7)

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