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Sterile Adhesive Plaster

by RFX+CARE Manufacturing Co., Ltd. EUDAMED

Active European Union

Ref FA200-9012Model 7.2 x 1.9 cm, 7.2 x 2.5 cm, 5.6x 1.9cm, etc.

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number69228209MDN1204IS0000337L Basic UDI-DIDate5 Sep 2022RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Certificates

0 certificates · EUDAMED

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

Specification

EUDAMED

Model / Reference
7.2 x 1.9 cm, 7.2 x 2.5 cm, 5.6x 1.9cm, etc., FA200-9012
Primary DI / UDI-DI
06922820990122
Basic UDI-DI
69228209MDN1204IS0000337L
Unit of Use DI
86922820990128
EMDN Code
M0599 Medical plasters - other
Device Class
Class I
Market of Registration
Denmark

Manufacturer details

EUDAMED SRN
CN-MF-000002971
Authorised representative
RFX+Care International A/S DK-AR-000001768

Other devices from RFX+CARE Manufacturing Co., Ltd.

See all devices from RFX+CARE Manufacturing Co., Ltd. →

Properties

  • Sterile
  • Contains Latex

Other properties (11)

  • Implantable: No
  • Reusable: 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