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MSI Precision Specialty Instruments IVD11120

by Med Saver, Inc.

MSI Precision Specialty Instruments IVD11120 is a Class I device made by Med Saver, Inc., listed in FDA GUDID since 1 Aug 2025 (UDI-DI 00194613037871), 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 Number00194613037871 UDI-DI Date1 Aug 2025ListedStatusListed 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  • Withdrawn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 joint/limb rongeur
Model / reference
IVD11120
Primary DI / UDI-DI
00194613037871
FDA product code
HTX
GMDN term
Orthopaedic joint/limb 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: Orthopaedic joint/limb rongeur

Similar devices in this category

Other devices filed under Orthopaedic joint/limb rongeur.

Other devices from Med Saver, Inc.

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Properties

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