Skip to content

Kmi Imi Group 19-0093

by Innovative Med, Inc.

Kmi Imi Group 19-0093 is a Class I device made by Innovative Med, Inc., listed in FDA GUDID since 30 Jan 2017 (UDI-DI 00851314007120), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00851314007120 UDI-DI Date30 Jan 2017ListedStatusListed 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  • Withdrawn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
Kmi Imi Group
Generic name
Open-surgery dissector
Model / reference
19-0093
Primary DI / UDI-DI
00851314007120
FDA product code
GDI
GMDN term
Open-surgery dissector
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Open-surgery dissector

Similar devices in this category

Other devices filed under Open-surgery dissector.

Other devices from Innovative Med, Inc.

See all devices from Innovative Med, Inc. →

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Serial number
  • Manufacturing date
Other properties (9, all answered No)