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Life Instruments 831-1233-3-1

by Life Instrument Corporation

Life Instruments 831-1233-3-1 is a Class I device made by Life Instrument Corporation, listed in FDA GUDID since 1 Mar 2021 (UDI-DI M9308311233310), 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 NumberM9308311233310 UDI-DI Date1 Mar 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  • Withdrawn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
Spinal rongeur
Model / reference
831-1233-3-1
Primary DI / UDI-DI
M9308311233310
FDA product code
HTX
GMDN term
Spinal rongeur
Device class
Class I
Regulation number
888.4540
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Spinal rongeur

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)