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Bard 0118003

by Davol 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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00801741031120 UDI-DI Date16 May 2015ListedStatusListed 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  • Withdrawn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
Bard
Generic Name
Extra-gynaecological surgical mesh, synthetic polymer, non-bioabsorbable
Model / Ref / Catalog
0118003
Description
Bard CK Parastomal Hernia Patch Size: 6.1" x 8.1" Stoma Opening Diameter: 1.1"-1.4"
Primary DI / UDI-DI
00801741031120
FDA Product Code
FTL
GMDN Term
Extra-gynaecological surgical mesh, synthetic polymer, non-bioabsorbable
Device Class
Class II
Regulation Number
878.3300
GUDID distribution status
Not in Commercial Distribution
Size
Width — 8.1 Inch
Length — 6.1 Inch

Other devices from Davol Inc.

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Properties

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

Other properties (8)

  • 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