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Destroject AD 1000 Syringe 0.5ml with Fixed Needle

by Amson Vaccines & Pharma (Pvt) Ltd. EUDAMED

Withdrawn No longer placed on the EU market

Ref 06-01-0001

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number896400331506-01-0001DT Basic UDI-DIDate29 May 2026RegisteredStatusWithdrawn No longer placed on the EU market

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDR Withdrawn

Certificates: none listed in EUDAMED

Specification

EUDAMED

Model / Reference
06-01-0001
Primary DI / UDI-DI
89640033150784
Basic UDI-DI
896400331506-01-0001DT
Direct Marketing DI
89640033150784
EMDN Code
A020199 Syringes, single-use - other
Device Class
Class IIa

Manufacturer details

EUDAMED SRN
PK-MF-000033205
Authorised representative
Obelis s.a. BE-AR-000000106

Properties

  • Sterile
  • Administering Medicine

Other properties (11)

  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No