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Penguin Newborn Suction

by Laerdal Medical AS 3 variants

Ref 98600060Model Penguin Newborn Suction

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number0704543209944T4 Basic UDI-DI 07045432047233UDI-DIDate24 Oct 2022RegisteredStatusActive

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  • Withdrawn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

Model / Reference
Penguin Newborn Suction, 98600060
Primary DI / UDI-DI
07045432047233
Basic UDI-DI
0704543209944T4
Direct Marketing DI
07045432047233
EMDN Code
L030101 Suction and irrigation surgical cannulas and handpieces, reusable
Device Class
Class I
EU market of registration
Norway

Manufacturer details

EUDAMED SRN
NO-MF-000000012

Other devices from Laerdal Medical AS

See all devices from Laerdal Medical AS →

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