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Surgical packs

by Jiangsu Medplus Non-woven Manufacturer Co., Ltd. 5 variants

Ref 25577Model ANGIOGRAPHIC PROCEDURE PACK

Active European Union

CE MDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-06971705249909 Basic UDI-DI 06971705249909UDI-DIDate6 Jul 2023RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDD Active

Specification

EUDAMED

Model / Reference
ANGIOGRAPHIC PROCEDURE PACK, 25577
Primary DI / UDI-DI
06971705249909
Basic UDI-DI
B-06971705249909
EMDN Code
T0203 Dressing and assistance kits
Device Class
Class I
EU market of registration
France

Manufacturer details

EUDAMED SRN
CN-MF-000022548
Authorised representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Other devices from JiangSu MedPlus Non-Woven Manufacturer Co., Ltd

See all devices from JiangSu MedPlus Non-Woven Manufacturer Co., Ltd →

Properties

  • Sterile

Other properties (10)

  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No