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MicroAire® 5740-200

by MicroAire Surgical Instruments LLC

MicroAire® 5740-200 is a Class II device made by MicroAire Surgical Instruments LLC, listed in FDA GUDID since 4 Aug 2016 (UDI-DI 00847399004093), 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 Number00847399004093 UDI-DI Date4 Aug 2016ListedStatusListed 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  • Withdrawn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
MicroAire®
Generic name
Surgical/orthopaedic lavage control unit
Model / reference
5740-200
Primary DI / UDI-DI
00847399004093
FDA product code
FQH
GMDN term
Surgical/orthopaedic lavage control unit
Device class
Class II
Regulation number
880.5475
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Surgical/orthopaedic lavage control unit

Similar devices

Other devices filed under FDA product code FQH (Lavage, Jet).

Other devices from MicroAire Surgical Instruments LLC

See all devices from MicroAire Surgical Instruments LLC →

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Serial number
  • Manufacturing date
Other properties (10, all answered No)