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Acardelta Tumbler

by Karapharm 7 variants

Ref 3675603Model Acar-Housses

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number376036425ACARHOUSSESPJ Basic UDI-DI 37603642503010UDI-DIDate23 Mar 2022RegisteredStatusActive EUDAMED: not on the EU market

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  • Withdrawn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
Housse complète anti-acarien pour personnes allergiques; fermée par une fermeture à glissière ; tissus 100% polyester
Model / Reference
Acar-Housses, 3675603
Primary DI / UDI-DI
37603642503010
Basic UDI-DI
376036425ACARHOUSSESPJ
EMDN Code
V9099 Various devices not included in other classes - other
Device Class
Class I

Manufacturer details

EUDAMED SRN
FR-MF-000006596

Other devices from Karapharm

See all devices from Karapharm →

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