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Bard® Guidewires 082438

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00801741052897 UDI-DI Date28 Jul 2017ListedStatusListed 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  • Withdrawn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
Bard® Guidewires
Generic Name
Gastro-urological guidewire, single-use
Model / Ref / Catalog
082438
Primary DI / UDI-DI
00801741052897
FDA Product Code
EZB
GMDN Term
Gastro-urological guidewire, single-use
Device Class
Class I
Regulation Number
876.5130
GUDID distribution status
In Commercial Distribution
Size
Length — 145 Centimeter
Outer Diameter — .038 Inch

Related devices

Category: Gastro-urological guidewire, single-use

Other devices from C. R. Bard, Inc.

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

Properties

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

Other properties (9)

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