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Exactamed H9387105

by Baxter Healthcare Corp

Exactamed H9387105 is a Class I device made by Baxter Healthcare Corp, listed in FDA GUDID since 24 Sep 2020 (UDI-DI 00085412478029), 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 Number00085412478029 UDI-DI Date24 Sep 2020ListedStatusListed 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  • Withdrawn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
Exactamed
Generic name
ENFit oral/enteral syringe, single-use
Model / Ref / Catalog
H9387105
Primary DI / UDI-DI
00085412478029
FDA product code
KYX
GMDN term
ENFit oral/enteral syringe, single-use
Device class
Class I
Regulation number
880.6430
GUDID distribution status
In Commercial Distribution
Size
Total Volume — 5 Milliliter

Related devices

Category: ENFit oral/enteral syringe, single-use

Similar devices in this category

Other devices filed under ENFit oral/enteral syringe, single-use.

Other devices from Baxter Healthcare Corp

See all devices from Baxter Healthcare Corp →

Properties

  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (11, all answered No)