Skip to content

Go-PAP

by Pulmodyne, Inc.

Ref 313-4605

Go-PAP (313-4605) is a Class IIa device made by Pulmodyne Inc., registered in EUDAMED on 29 Oct 2026 (Basic UDI-DI B-00841470111786), active as of 7 Nov 2026.

Active European Union

CE MDD

Valid until

No date given

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

Source EUDAMED, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-00841470111786 Basic UDI-DI 00841470111786UDI-DIDate29 Oct 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Model / reference
313-4605
Primary DI / UDI-DI
00841470111786
Basic UDI-DI
B-00841470111786
EMDN code
Z12030102 Continuous positive pressure equipment
Device class
Class IIa
EU registration type
Legacy device (under a directive)
EU market of registration
Lithuania

Manufacturer details

EUDAMED SRN
US-MF-000017334
Authorised representative
QNET B.V. NL-AR-000002695

Similar devices in this category

Other devices filed under CONTINUOUS POSITIVE PRESSURE EQUIPMENT.

Other devices from Pulmodyne Inc.

See all devices from Pulmodyne Inc. →

Properties

Other properties (12, all answered No)