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MicroVENT Industrial resuscitation kit with soft case.

by B.N.O.S. Meditech Limited

Ref 670-0309-01

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 linked in EUDAMED

A group certificate may exist

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 Number5052270EMERGENCYKITMV9M Basic UDI-DI 05052270000018UDI-DIDate12 Sep 2023RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
MicroVENT
Model / Reference
670-0309-01
Primary DI / UDI-DI
05052270000018
Basic UDI-DI
5052270EMERGENCYKITMV9M
EMDN Code
V0501 Clinical emergency kits
Device Class
Class IIb
Medical Purpose
System designed for professional emergency services use when breathing has stopped, when breathing assistance is needed or if oxygen therapy is required.

Manufacturer details

EUDAMED SRN
UK-PR-000037512

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Properties

Other properties (1)

  • Sterile: No