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Clinofar

by Laboratoire de la Mer 2 variants

Ref OH2119000Model LABMER-007/A-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, 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 Number356430LABMER-007/A-HT Basic UDI-DI 03564300031852UDI-DIDate29 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  • Withdrawn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
Baby Nasal Aspirator & Pack of single-use filters
Model / Reference
LABMER-007/A-01, OH2119000
Primary DI / UDI-DI
03564300031852
Basic UDI-DI
356430LABMER-007/A-HT
EMDN Code
Q030199 Nasopharyngeal devices - other
Device Class
Class I
EU market of registration
Greece

Manufacturer details

EUDAMED SRN
FR-MF-000009050

Other devices from Laboratoire de la Mer

See all devices from Laboratoire de la Mer →

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