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EasyTouch 832531

by MHC Medical Products

EasyTouch 832531 is a Class II device made by MHC Medical Products, listed in FDA GUDID since 4 Aug 2016 (UDI-DI MHC18325311), 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 NumberMHC18325311 UDI-DI Date4 Aug 2016ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
EasyTouch
Generic name
Insulin syringe/needle, basic
Model / reference
832531
Primary DI / UDI-DI
MHC18325311
FDA product code
MEG
GMDN term
Insulin syringe/needle, basic
Device class
Class II
Regulation number
880.5860
GUDID distribution status
In Commercial Distribution
Sterilisation method
Ethylene Oxide

Related devices

Category: Insulin syringe/needle, basic

Similar devices

Other devices filed under FDA product code MEG (Syringe, Antistick).

Other devices from MHC Medical Products

See all devices from MHC Medical Products →

Properties

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