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I-Scoop Video laryngoscope/Model: I-Scoop 200

by Hebei Vimed Medical Device Company, LTD

Ref 2400000Model 2111000

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 Number6971834830002AX Basic UDI-DI 06971834831334UDI-DIDate16 Jun 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  • Withdrawn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
Pocket VL video laryngoscope PVL-I-01 Plus (pediatric)
Model / Reference
2111000, 2400000
Primary DI / UDI-DI
06971834831334
Basic UDI-DI
6971834830002AX
Direct Marketing DI
06971834831334
EMDN Code
Z12021004 Video laryngoscopes
Device Class
Class I
EU market of registration
France

Manufacturer details

EUDAMED SRN
CN-MF-000002086
Authorised representative
Supporting Health Care N.V. NL-AR-000001835

Other devices from Hebei Vimed Medical Device Company, Ltd.

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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