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Life Instruments 792-1206-B32

by Life Instrument Corporation

Part of a family of 29 devices: see the family page

Ref 792-1206-B32

Life Instruments 792-1206-B32 is a Class I device made by Life Instrument Corporation, registered in EUDAMED on 31 Mar 2026 (Basic UDI-DI ++M930012PY) and listed in FDA GUDID since 17 Feb 2022 (UDI-DI M9307921206B320), active as of 23 Oct 2026.

Active European Union. Also listed in GUDID (US).

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number++M930012PY Basic UDI-DI M9307921206B320UDI-DIDate31 Mar 2026RegisteredStatusActive
United StatesGUDID listing GUDID NumberM9307921206B320 UDI-DI Date17 Feb 2022ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI ++M930012PY registered 31 Mar 2026 Active
  • FDA GUDID UDI-DI M9307921206B320 listed 17 Feb 2022 Listed

Timeline

2 dated events

  1. Listed FDA GUDID M9307921206B320
  2. Registered EUDAMED ++M930012PY

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade name
Guide EUDAMED
Life Instruments GUDID
Generic name
Orthopaedic surgical distractor, external
Device name
General Surgical Instruments
Model / reference
792-1206-B32
Primary DI / UDI-DI
M9307921206B320
Basic UDI-DI
++M930012PY
FDA product code
LXH
EMDN code
L0399 General surgery instruments, reusable - other
GMDN term
Orthopaedic surgical distractor, external
Device class
Class I
Regulation number
888.4540
EU registration type
Standard device
EU market of registration
Spain
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Orthopaedic surgical distractor, external

Similar devices in this category

Other devices filed under GENERAL SURGERY INSTRUMENTS, REUSABLE.

Other devices from Life Instrument Corporation

See all devices from Life Instrument Corporation →

Properties

  • Sterilise before use
  • Reusable
  • Premarket exempt
Other properties (22, all answered No)