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Erka. Precise

by ERKA Kallmeyer Medizintechnik GmbH & Co. Kommanditgesellschaft Germany EUDAMED

Ref 531.00083.7590Model Precise

EMDN C9005

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number42502961531LM Basic UDI-DIDate26 Sep 2025RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Not covered

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 24 Oct 2026

Device Name
Precise
Model / Reference
Precise, 531.00083.7590
Primary DI / UDI-DI
04250296180351
Basic UDI-DI
42502961531LM
EMDN Code
C9005 Phonendoscopes and stethoscopes
Device Class
Class I
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000009663

Other devices from ERKA Kallmeyer Medizintechnik GmbH & Co. Kommanditgesellschaft

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Properties & raw data

Show properties, registry sources and raw records
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

Sources (1)

  • EUDAMED 5644d4b3-0457-48fa-bbba-680778dc735d 61 fields · synced 24 Oct 2026