Skip to content

Equashield Syringe Unit

by Equashield Medical Ltd 24 variants

Equashield Syringe Unit is a Class II device made by Equashield Medical Ltd, listed in FDA GUDID since 16 May 2016 (UDI-DI 07290013484277), 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 Number07290013484277 UDI-DI Date16 May 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  • Withdrawn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
Equashield
Generic name
Medication transfer set
Model / reference
Equashield Syringe Unit
Primary DI / UDI-DI
07290013484277
FDA product code
ONB
GMDN term
Medication transfer set
Device class
Class II
Regulation number
880.5440
GUDID distribution status
In Commercial Distribution

Related devices

Category: Medication transfer set

Similar devices

Other devices filed under FDA product code ONB (Closed Antineoplastic And Hazardous Drug Reconstitution And Transfer System).

Other devices from Equashield Medical Ltd

See all devices from Equashield Medical Ltd →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)