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Aneroid Sphygmomanometer

by Microlife Corporation EUDAMED

Active European Union

Ref BP AG1-30

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number4719003ANRR Basic UDI-DIDate8 May 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  • Withdrawn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

Device Name
Aneroid Sphygmomanometer
Model / Reference
BP AG1-30
Primary DI / UDI-DI
04719003689452
Basic UDI-DI
4719003ANRR
EMDN Code
C9006 Aneroid sphygmomanometers
Device Class
Class I
Market of Registration
Lithuania

Manufacturer details

EUDAMED SRN
TW-MF-000010688
Authorised representative
Microlife UAB LT-AR-000011673

Other devices from Microlife Corporation

See all devices from Microlife Corporation →

Properties

  • 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