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MSI Precision Specialty Instruments D7406

by Med Saver, Inc.

MSI Precision Specialty Instruments D7406 is a Class I device made by Med Saver, Inc., listed in FDA GUDID since 15 Aug 2024 (UDI-DI 00194613079680), 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 Number00194613079680 UDI-DI Date15 Aug 2024ListedStatusListed 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  • Withdrawn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 Precision Specialty Instruments
Generic name
Orthopaedic bone-fragment manipulator, reusable
Model / reference
D7406
Primary DI / UDI-DI
00194613079680
FDA product code
GEN
GMDN term
Orthopaedic bone-fragment manipulator, 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: Orthopaedic bone-fragment manipulator, reusable

Other devices from Med Saver, Inc.

See all devices from Med Saver, Inc. →

Properties

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