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DNlite-IVD103

by Bio Preventive Medicine Corp. 2 variants

Ref 8103106 (4oC)

Active European Union

CE IVDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number471987949E103017J Basic UDI-DI 04719879490664UDI-DIDate17 Oct 2022RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/IVDR Active

Specification

EUDAMED

Device Name
DNlite uPTM-FetA ELISA Kit
Model / Reference
8103106 (4oC)
Primary DI / UDI-DI
04719879490664
Basic UDI-DI
471987949E103017J
EMDN Code
W0102019099 Specific proteins - other
Device Class
Class B
EU market of registration
Czechia

Manufacturer details

EUDAMED SRN
TW-MF-000022845
Authorised representative
Emergo Europe B.V. NL-AR-000000116

Other devices from Bio Preventive Medicine Corp.

Properties

  • Animal Tissues
  • Reagent
  • Professional Testing

Other properties (8)

  • Sterile: No
  • Human Tissues: No
  • Microbial Substances: No
  • Self Testing: No
  • Near-Patient Testing: No
  • Companion Diagnostics: No
  • Surgical Instrument: No
  • New Device: No