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HeartView

by Aerotel Medical Systems (1998) Ltd. 4 variants

Ref P12/8i

Active European Union

CE MDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-HeartView-P12/8i26 Basic UDI-DI D-HeartView-P12/8i26UDI-DIDate31 Oct 2023RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDD Active

Specification

EUDAMED

Device Name
HeartView
Model / Reference
P12/8i
Primary DI / UDI-DI
D-HeartView-P12/8i26
Basic UDI-DI
B-HeartView-P12/8i26
EMDN Code
Z12050403 ECG holter recorders
Device Class
Class IIa
EU market of registration
Ireland

Manufacturer details

EUDAMED SRN
IL-MF-000038449
Authorised representative
AF Pharma Service Europe SL ES-AR-000018076

Other devices from Aerotel Medical Systems (1998) Ltd.

See all devices from Aerotel Medical Systems (1998) Ltd. →

Properties

  • Measuring Function

Other properties (10)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Incorporates Medicinal Product: No