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Waterproof drape with 4 aperture (2 Radials and 2 Femoral) 260x340cm with reinforcement and 2 transparent banners (80cm)

by Adhe-Els SA.

Ref CH-ANGIO-009Model Clothing, draping and care sets NEODRAP

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-CH-ANGIO-009PA Basic UDI-DI D-CH-ANGIO-009PAUDI-DIDate12 May 2025RegisteredStatusActive

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  • Withdrawn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

Device Name
NEODRAP®Waterproof drape with 4 aperture (2 Radials and 2 Femoral) 260x340cm with reinforcement and 2 transparent banners (80cm)
Model / Reference
Clothing, draping and care sets NEODRAP, CH-ANGIO-009
Primary DI / UDI-DI
D-CH-ANGIO-009PA
Basic UDI-DI
B-CH-ANGIO-009PA
EMDN Code
T020102, T020199
Device Class
Class I
EU market of registration
France

Manufacturer details

EUDAMED SRN
TN-MF-000011757
Authorised representative
ADHE-ELS FRANCE FR-AR-000001654

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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