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Msi 742-12

by Modern Surgical Instruments LLC

Msi 742-12 is a Class I device made by Modern Surgical Instruments LLC, listed in FDA GUDID since 30 Mar 2023 (UDI-DI 00810130201860), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00810130201860 UDI-DI Date30 Mar 2023ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Msi
Generic name
Orthopaedic surgical distractor, external
Model / reference
742-12
Primary DI / UDI-DI
00810130201860
FDA product code
GAD
GMDN term
Orthopaedic surgical distractor, external
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Similar devices

Other devices filed under FDA product code GAD (Retractor).

Other devices from Modern Surgical Instruments LLC

See all devices from Modern Surgical Instruments LLC →

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (11, all answered No)