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Plus A3

by Medi̇kal 2000 Tibbi̇ Ci̇hazlar Ve İleri̇ Teknoloji̇ San. Ve Ti̇c. A.Ş.

Ref PLUS A3

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 Number86976015PLUSA35T Basic UDI-DI 08697601520635UDI-DIDate18 Oct 2026RegisteredStatusActive

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  • Withdrawn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
Plus A3 Electromechanic Hospital Bed
Model / Reference
PLUS A3
Primary DI / UDI-DI
08697601520635
Basic UDI-DI
86976015PLUSA35T
EMDN Code
V08060101 Hospital/home care electric medical beds
Device Class
Class I
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
TR-MF-000019533

Other devices from Medi̇kal 2000 Tibbi̇ Ci̇hazlar Ve İleri̇ Teknoloji̇ San. Ve Ti̇c. A.Ş.

See all devices from Medi̇kal 2000 Tibbi̇ Ci̇hazlar Ve İleri̇ Teknoloji̇ San. Ve Ti̇c. A.Ş. →

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