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1p/19q gene deletion detection probe - 1p/19q gene deletion detection probe (1P36/1q25

by Oacp Ie Ltd

Ref FP-045

Active European Union

CE IVDD

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/IVDD NumberB-5391540380FP-045T84Z Basic UDI-DI D-5391540380FP-045T84ZUDI-DIDate21 Dec 2025RegisteredStatusActive

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  • Withdrawn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/IVDD Active

Specification

EUDAMED

Device Name
1p/19q gene deletion detection probe (1P36/1q25 ; 19q13/19p13)
Model / Reference
FP-045
Primary DI / UDI-DI
D-5391540380FP-045T84Z
Basic UDI-DI
B-5391540380FP-045T84Z
EMDN Code
W01030703 DNA in situ hybridisation reagents
Models / Variants
1p/19q gene deletion detection probe (1P36/1q25
Device Class
Class IVD General
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
IE-MF-000003506

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Properties

  • Reagent
  • Professional Testing

Other properties (8)

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