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Physiomer

by Laboratoire de la Mer 10 variants

Ref OH21132020Model LABMER-002/D-01

Active European Union

CE MDD

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/MDD NumberB-08710537044546 Basic UDI-DI 08710537044546UDI-DIDate29 Mar 2024RegisteredStatusActive

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  • Withdrawn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/MDD Active

Specification

EUDAMED

Device Name
Physiomer NL HYPERTONIC 20ML
Model / Reference
LABMER-002/D-01, OH21132020
Primary DI / UDI-DI
08710537044546
Basic UDI-DI
B-08710537044546
EMDN Code
Q030103 Nasal irrigation solutions
Device Class
Class I
EU market of registration
Netherlands

Manufacturer details

EUDAMED SRN
FR-MF-000009050

Other devices from Laboratoire de la Mer

See all devices from Laboratoire de la Mer →

Properties

  • Sterile

Other properties (10)

  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No