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Baxter 0600128

by Micromedics, Inc.

Baxter 0600128 is a medical device (FDA Class II; FDA product code FMF, Syringe, Piston) made by Micromedics, Inc., listed in FDA GUDID since 15 Apr 2021 (UDI-DI 00815634020863), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00815634020863 UDI-DI Date15 Apr 2021ListedStatusListed 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  • Withdrawn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
Baxter
Generic name
Fibrin sealant biochemical preparation/application kit, endoscopic
Model / reference
0600128
Primary DI / UDI-DI
00815634020863
FDA product code
FMF
GMDN term
Fibrin sealant biochemical preparation/application kit, endoscopic
Device class
Class II
Regulation number
880.5860
GUDID distribution status
In Commercial Distribution

Related devices

Category: Fibrin sealant biochemical preparation/application kit, endoscopic

Similar devices

Other devices filed under FDA product code FMF (Syringe, Piston).

Other devices from Micromedics, Inc.

See all devices from Micromedics, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Serial number
  • Expiration date
Other properties (9, all answered No)