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Plaster Stripe

by Miracle Medical Industries

Ref 6222012027507, PLASTER STRIPE TRANSPERENT

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 Number6222012027507MU Basic UDI-DI Date14 Feb 2023RegisteredStatusActive

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  • Withdrawn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

Trade Name
Miracle PLASTER STRIPE TRANSPERENT
Device Name
Plaster Stripe
Model / Reference
6222012027507, PLASTER STRIPE TRANSPERENT
Primary DI / UDI-DI
06222012027507, 06222012008827
Basic UDI-DI
6222012027507MU
EMDN Code
M050199 Surgical plasters - other
Device Class
Class I
EU market of registration
Spain
Bulgaria

Manufacturer details

EUDAMED SRN
EG-MF-000032514
Authorised representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Other devices from Miracle Medical Industries

See all devices from Miracle Medical Industries →

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