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Set Tunnelgleithilfe - 2er Set ca. 35 x 65 cm - offen auf 65 cm, 100 % Nylon, silikonbeschichtet

by Centre Barbara Schardt e.K.

Ref 51140 SModel Centre Gleithilfen

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number42519946GLEITHILFENZT Basic UDI-DI 04251994650061UDI-DIDate21 Jul 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  • Withdrawn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
Centre Gleithilfen
Model / Reference
Centre Gleithilfen, 51140 S
Primary DI / UDI-DI
04251994650061
Basic UDI-DI
42519946GLEITHILFENZT
EMDN Code
Z12019010 Patient transfer systems
Device Class
Class I
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000021441

From the manufacturer

Manufacturer's product page: Sets (15)

Other devices from Centre Barbara Schardt e.K.

See all devices from Centre Barbara Schardt e.K. →

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