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AtiX Sprej na bezpečné odstraňovanie kliešťov/

by JM Sante Pharma Spółka z ograniczoną odpowiedzialnością

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 Number590259671801GE Basic UDI-DI 05902596718060UDI-DIDate16 Apr 2026RegisteredStatusActive

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  • Withdrawn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
AtiX Sprej na bezpečné odstraňovanie kliešťov/Sprej pro bezpečné odstraňování klíšťat
Primary DI / UDI-DI
05902596718060
Basic UDI-DI
590259671801GE
Direct Marketing DI
05902596718060
EMDN Code
V901099 Parasite elimination mechanical devices - other
Device Class
Class I
EU market of registration
Czechia

Manufacturer details

EUDAMED SRN
PL-MF-000007174

Other devices from JM Sante Pharma Spółka z ograniczoną odpowiedzialnością

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