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Life Instruments 741-1230-2-2

by Life Instrument Corporation

Life Instruments 741-1230-2-2 is a Class I device made by Life Instrument Corporation, listed in FDA GUDID since 19 Oct 2021 (UDI-DI M9307411230220), 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 NumberM9307411230220 UDI-DI Date19 Oct 2021ListedStatusListed 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  • Withdrawn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
Life Instruments
Generic name
Self-retaining surgical retractor, reusable
Model / reference
741-1230-2-2
Primary DI / UDI-DI
M9307411230220
FDA product code
GAD
GMDN term
Self-retaining surgical retractor, reusable
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Self-retaining surgical retractor, reusable

Other devices from Life Instrument Corporation

See all devices from Life Instrument Corporation →

Properties

  • Sterilise before use
  • Premarket exempt
Other properties (13, all answered No)