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Elmed Incorporated 23-1021SLH

by Elmed Incorporated

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 Number00198506087073 UDI-DI Date17 Dec 2025ListedStatusListed 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  • Withdrawn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
Elmed Incorporated
Generic Name
Arthroscopic surgical procedure kit, non-medicated, reusable
Model / Ref / Catalog
23-1021SLH
Description
GRASPING FORCEPS - ALLIGATOR 2.7 UPBITER SLIDE LOCK HANDLE UPSWEPT
Primary DI / UDI-DI
00198506087073
FDA Product Code
NBH
GMDN Term
Arthroscopic surgical procedure kit, non-medicated, reusable
Device Class
Class I
Regulation Number
888.1100
GUDID distribution status
In Commercial Distribution
Sterilization Method
Moist Heat or Steam Sterilization

Other devices from Elmed Incorporated

See all devices from Elmed Incorporated →

Properties

  • Prescription Use
  • Premarket Exempt
  • Lot / Batch Number
  • Manufacturing Date

Other properties (10)

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