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PEEP Valves

by Intersurgical Ltd 8 variants

Ref 2226000

PEEP Valves (2226000) is a Class IIa device made by Intersurgical Ltd, registered in EUDAMED on 4 Nov 2026 (Basic UDI-DI 05030267PVALVECF), active as of 7 Nov 2026.

Active European Union

CE MDR

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/MDR Number05030267PVALVECF Basic UDI-DI 05030267094349UDI-DIDate4 Nov 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device name
PEEP Valves
Model / reference
2226000
Primary DI / UDI-DI
05030267094349
Basic UDI-DI
05030267PVALVECF
Unit of use DI
05030267098835
EMDN code
R028001 Respiratory circuits valves
Device class
Class IIa
EU registration type
Standard device
EU market of registration
Belgium

Manufacturer details

EUDAMED SRN
GB-MF-000004798
Authorised representative
UAB Intersurgical LT-AR-000003907

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Other devices filed under RESPIRATORY CIRCUITS VALVES.

Other devices from Intersurgical Ltd

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Properties

Other properties (14, all answered No)