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hydrocolloid blister plaster

by Ningbo Chinmed Technology Co., Ltd 2 variants

Model FL-YB&FL-CB&FL-DX

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number697286436600006B Basic UDI-DI 06972864367992UDI-DIDate6 Jun 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  • Withdrawn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
hydrocolloid plaster
Model / Reference
FL-YB&FL-CB&FL-DX
Primary DI / UDI-DI
06972864367992
Basic UDI-DI
697286436600006B
EMDN Code
M0599 Medical plasters - other
Device Class
Class I
EU market of registration
Finland

Manufacturer details

EUDAMED SRN
CN-MF-000023983
Authorised representative
SUNGO Europe B.V. NL-AR-000000247

Other devices from Ningbo Chinmed Technology Co., Ltd.

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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