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Biogel 71-75275

by Bosma Enterprises

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 Number10818634024081 UDI-DI Date1 Jul 2021ListedStatusListed 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  • Withdrawn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
Biogel
Generic name
Hevea-latex surgical glove, non-powdered, non-antimicrobial
Model / Ref / Catalog
71-75275
Primary DI / UDI-DI
10818634024081
FDA product code
KGO
GMDN term
Hevea-latex surgical glove, non-powdered, non-antimicrobial
Device class
Class I
Regulation number
878.4460
GUDID distribution status
Not in Commercial Distribution

Related devices

Category: Hevea-latex surgical glove, non-powdered, non-antimicrobial

Other devices from Bosma Enterprises

See all devices from Bosma Enterprises →

Properties

  • Supplied sterile
  • Single use
  • Contains latex
  • Lot / batch number
  • Expiration date

Other properties (10)

  • Sterilise before use: No
  • Implantable: No
  • Prescription use: No
  • Over-the-counter: No
  • Convenience kit: No
  • Combination product: No
  • HCT/P: No
  • Premarket exempt: No
  • Serial number: No
  • Manufacturing date: No