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Pd Detect I

by AIDA GmbH Germany EUDAMED

Ref SAA-001_02, SAA-001_20

EMDN W01019099

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number42601586PDDETECTSE Basic UDI-DIDate2 Apr 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Not covered

European Union — CE/IVDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 22 Oct 2026

Device Name
Pd Detect
Model / Reference
SAA-001_02, SAA-001_20
Primary DI / UDI-DI
04260158683531, 04260158683500
Basic UDI-DI
42601586PDDETECTSE
EMDN Code
W01019099 Clinical chemistry reagents - other
Device Class
Class B
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000040784

Related devices

Category: Nucleic acid extraction/isolation kit IVD

Other devices from AIDA GmbH

See all devices from AIDA GmbH →

Properties & raw data

Show properties, registry sources and raw records
  • Human Tissues
  • Microbial Substances
  • Professional Testing
  • New Device
Other properties (7)
  • Sterile: No
  • Animal Tissues: No
  • Reagent: No
  • Self Testing: No
  • Near-Patient Testing: No
  • Companion Diagnostics: No
  • Surgical Instrument: No

Sources (2)

  • EUDAMED ba57dcaa-b260-43d1-8752-d026c2abfab6 61 fields · synced 22 Oct 2026
  • EUDAMED 04260158683500|42601586PDDETECTSE 61 fields · synced 19 May 2026