Skip to content

MSI Precision Specialty Instruments 91573515

by Med Saver, Inc.

MSI Precision Specialty Instruments 91573515 is a Class I device made by Med Saver, Inc., listed in FDA GUDID since 1 Aug 2025 (UDI-DI 00194613115906), 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 Number00194613115906 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  • Withdrawn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
Periosteal elevator, reusable
Model / reference
91573515
Primary DI / UDI-DI
00194613115906
FDA product code
LXH
GMDN term
Periosteal elevator, reusable
Device class
Class I
Regulation number
888.4540
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Periosteal elevator, 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)