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Msi MAX9003

by Modern Surgical Instruments LLC

Msi MAX9003 is a Class I device made by Modern Surgical Instruments LLC, listed in FDA GUDID since 12 Feb 2025 (UDI-DI 00850017626362), 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 Number00850017626362 UDI-DI Date12 Feb 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  • Withdrawn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
Generic name
General-purpose light source
Model / reference
MAX9003
Primary DI / UDI-DI
00850017626362
FDA product code
MDM
GMDN term
General-purpose light source
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution

Related devices

Category: General-purpose light source

Similar devices

Other devices filed under FDA product code MDM (Instrument, Manual, Surgical, General Use).

Other devices from Modern Surgical Instruments LLC

See all devices from Modern Surgical Instruments LLC →

Properties

  • Premarket exempt
  • Lot / batch number
Other properties (13, all answered No)