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Pulsenmore ES

by Pulsenmore Ltd 3 variants

Ref 800-0013Model 400-0001

Active European Union

CE MDR

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number7290018579PulsenmoreESLC Basic UDI-DI 07290018579077UDI-DIDate19 Jan 2026RegisteredStatusActive

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  • Withdrawn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/MDR Active

Specification

EUDAMED

Device Name
Pulsemore ES
Model / Reference
400-0001, 800-0013
Primary DI / UDI-DI
07290018579077
Basic UDI-DI
7290018579PulsenmoreESLC
EMDN Code
Z11040106 Handheld ultrasound scanners
Device Class
Class IIa
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
IL-MF-000037891
Authorised representative
Medical Technology Promedt Consulting GmbH DE-AR-000000085

Other devices from Pulsenmore Ltd

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