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Life Instruments 749-2080-0B

by Life Instrument Corporation

Life Instruments 749-2080-0B is a Class I device made by Life Instrument Corporation, listed in FDA GUDID since 8 Feb 2022 (UDI-DI M93074920800B0), 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 NumberM93074920800B0 UDI-DI Date8 Feb 2022ListedStatusListed 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  • Withdrawn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
Surgical retractor/retraction system blade, reusable
Model / reference
749-2080-0B
Primary DI / UDI-DI
M93074920800B0
FDA product code
GAD
GMDN term
Surgical retractor/retraction system blade, 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: Surgical retractor/retraction system blade, reusable

Similar devices in this category

Other devices filed under Surgical retractor/retraction system blade, reusable.

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Properties

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