Skip to content

Mattress

by Pt Newlife Healthcare International

Ref NHI-M-001Model NHI-M-001,NHI-M-002,NHI-M-003,NHI-M-004,NHI-M-005

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number899446881M001QK Basic UDI-DI 08994468810047UDI-DIDate4 Feb 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  • Withdrawn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
Mattress
Model / Reference
NHI-M-001, NHI-M-002, NHI-M-003, NHI-M-004, NHI-M-005
Primary DI / UDI-DI
08994468810047
Basic UDI-DI
899446881M001QK
EMDN Code
V08068002 Bed supports
Device Class
Class I
EU market of registration
Austria

Manufacturer details

EUDAMED SRN
ID-MF-000051541
Authorised representative
SUNGO Europe B.V. NL-AR-000000247

Other devices from Pt Newlife Healthcare International

See all devices from Pt Newlife Healthcare International →

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