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Lm 3264 W

by Home Medical Service H.M.S.

Ref LM 3264 WModel HARMONIE TWICE

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, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number361580HARMONIETWICEHP Basic UDI-DI 03615800047765UDI-DIDate14 Feb 2025RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Lm 3060 W
Model / Reference
HARMONIE TWICE, LM 3264 W
Primary DI / UDI-DI
03615800047765
Basic UDI-DI
361580HARMONIETWICEHP
Direct Marketing DI
03615800047765
EMDN Code
V08060101 Hospital/home care electric medical beds
Device Class
Class I
EU market of registration
France

Manufacturer details

EUDAMED SRN
FR-MF-000028528

Other devices from Home Medical Service H.M.S.

See all devices from Home Medical Service H.M.S. →

Properties

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