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Kmedic IPN014862

by Teleflex Incorporated

Kmedic IPN014862 (KM49753) is a Class I device made by Teleflex Incorporated, listed in FDA GUDID since 15 Sep 2018 (UDI-DI 24026704282597), registry data as of 23 Oct 2026.

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

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number24026704282597 UDI-DI Date15 Sep 2018ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Kmedic
Generic name
Orthopaedic implant impactor, reusable
Model / Ref / Catalog
IPN014862, KM49753
Primary DI / UDI-DI
24026704282597
FDA product code
HWA
GMDN term
Orthopaedic implant impactor, reusable
Device class
Class I
Regulation number
888.4540
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization
Size
Length — 25 Centimeter

Related devices

Category: Orthopaedic implant impactor, reusable

Other devices from Teleflex Incorporated

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  • Arrow IPNB00827 Open recall

    Class II

See all devices from Teleflex Incorporated →

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (10, all answered No)