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Gelita-Spon® Standard Gs-210

by GELITA MEDICAL GmbH

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 Number04260293133106 UDI-DI Date27 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  • Withdrawn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
Gelita-Spon® Standard
Generic Name
Gelatin haemostatic agent
Model / Reference
GS-210
Primary DI / UDI-DI
04260293133106
FDA Product Code
LYA, KHJ
GMDN Term
Gelatin haemostatic agent
Device Class
Class I
Regulation Number
874.4780, 874.3620
GUDID distribution status
Not in Commercial Distribution
Size
Length — 80 Millimeter
Outer Diameter — 30 Millimeter

Properties

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

Other properties (7)

  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No