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Laryngoscope Snap-on, Set of 4 Miller Blades 1, 2, 3, 4 + LED Medium Handle

by Medical Devices (Pvt) Ltd 2 variants

Ref 810-905-03

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 Number896110278LRYRF810FU Basic UDI-DI 08961102782350UDI-DIDate25 Nov 2025RegisteredStatusActive

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  • Withdrawn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
Laryngoscope, Reusable
Model / Reference
810-905-03
Primary DI / UDI-DI
08961102782350
Basic UDI-DI
896110278LRYRF810FU
EMDN Code
Z12021003 Laryngoscopes
Device Class
Class I
EU market of registration
Czechia

Manufacturer details

EUDAMED SRN
PK-MF-000021845
Authorised representative
Obelis s.a. BE-AR-000000106

Related devices

Category: Laryngoscope blade, reusable

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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