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Apoteket Kirurgtejp Vit Ny 2025

by Suzhou Sunmed Co., Ltd.

Ref 215427

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

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/MDR Number697386485APOTEKTAPE97 Basic UDI-DI 06973864850590UDI-DIDate26 Dec 2024RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Tape
Model / Reference
215427
Primary DI / UDI-DI
06973864850590
Basic UDI-DI
697386485APOTEKTAPE97
EMDN Code
H900299 Tapes, medical/surgical - other
Device Class
Class I
EU market of registration
Sweden

Manufacturer details

EUDAMED SRN
CN-MF-000010170
Authorised representative
SUNGO Europe B.V. NL-AR-000000247

Other devices from Suzhou Sunmed Co., Ltd.

See all devices from Suzhou Sunmed Co., Ltd. →

Properties

Other properties (13)

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