Skip to content

Life Instruments 725-0913-0-1

by Life Instrument Corporation

Life Instruments 725-0913-0-1 is a Class I device made by Life Instrument Corporation, listed in FDA GUDID since 30 Apr 2021 (UDI-DI M9307250913010), 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 NumberM9307250913010 UDI-DI Date30 Apr 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  • Withdrawn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
Open-surgery dissector
Model / reference
725-0913-0-1
Primary DI / UDI-DI
M9307250913010
FDA product code
HXB
GMDN term
Open-surgery dissector
Device class
Class I
Regulation number
888.4540
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Open-surgery dissector

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)