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Dynablot

by DYNEX TECHNOLOGIES, spol. s r.o. EUDAMED

Active European Union

Ref D7130Model DYNABLOT

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number859421131027-71JQ Basic UDI-DIDate25 May 2026RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/IVDR Active

Certificates

0 certificates · EUDAMED

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

Specification

EUDAMED

Device Name
Dynablot
Model / Reference
DYNABLOT, D7130
Primary DI / UDI-DI
08594211310277
Basic UDI-DI
859421131027-71JQ
Direct Marketing DI
08594211310277
EMDN Code
W02050103 Blotting systems
Device Class
Class A
Market of Registration
Czechia

Manufacturer details

EUDAMED SRN
CZ-MF-000023791

Other devices from DYNEX TECHNOLOGIES, spol. s r.o.

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Properties

  • Human Tissues
  • Professional Testing
  • Surgical Instrument

Other properties (8)

  • Sterile: No
  • Animal Tissues: No
  • Microbial Substances: No
  • Reagent: No
  • Self Testing: No
  • Near-Patient Testing: No
  • Companion Diagnostics: No
  • New Device: No