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MSI Precision Specialty Instruments F9480

by Med Saver, Inc.

MSI Precision Specialty Instruments F9480 is a Class I device made by Med Saver, Inc., listed in FDA GUDID since 21 Mar 2025 (UDI-DI 00194613096274), 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 Number00194613096274 UDI-DI Date21 Mar 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  • Withdrawn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
General-purpose curette
Model / reference
F9480
Primary DI / UDI-DI
00194613096274
FDA product code
HTF
GMDN term
General-purpose curette
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: General-purpose curette

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)