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Erka. Kobold

by ERKA Kallmeyer Medizintechnik GmbH & Co. Kommanditgesellschaft Germany EUDAMED

Ref 223.20493.7290Model Kobold EMDN C9006

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number42502961223L7 Basic UDI-DIDate25 Sep 2025RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 23 Oct 2026

Device Name
Kobold
Model / Reference
Kobold, 223.20493.7290
Primary DI / UDI-DI
04250296150286
Basic UDI-DI
42502961223L7
EMDN Code
C9006 Aneroid sphygmomanometers
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
  • Measuring Function
Other properties (12)
  • 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
  • Incorporates Medicinal Product: No

Sources (1)

  • EUDAMED 235c3186-7331-4f7f-b9e5-51aca47b8c56 61 fields · synced 23 Oct 2026