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Nitrocare Manuel Hasta Karyolasi

by Nitrocare Medi̇kal Mobi̇lya Sanayi̇ Ve Ti̇caret Anoni̇m Şi̇rketi̇ 11 variants

Ref NITRO HB 1120Model NITRO HB 6440

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number869925869NTRCBEDMX Basic UDI-DI 08699258690532UDI-DIDate3 Apr 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  • Withdrawn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
Motorized Patient Bed
Model / Reference
NITRO HB 6440, NITRO HB 1120
Primary DI / UDI-DI
08699258690532
Basic UDI-DI
869925869NTRCBEDMX
Direct Marketing DI
08699258690532
EMDN Code
V080602 Manual medical beds
Device Class
Class I
EU market of registration
Türkiye

Manufacturer details

EUDAMED SRN
TR-MF-000044596

Other devices from Nitrocare Medi̇kal Mobi̇lya Sanayi̇ Ve Ti̇caret Anoni̇m Şi̇rketi̇

See all devices from Nitrocare Medi̇kal Mobi̇lya Sanayi̇ Ve Ti̇caret Anoni̇m Şi̇rketi̇ →

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