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Frenodiar SRO

by PHARMA LINE Srl

Ref PEESCATI0001Model Catridal 10 buste

Frenodiar SRO (PEESCATI0001) is a Class IIa device made by PHARMA LINE Srl, registered in EUDAMED on 2 Oct 2026 (Basic UDI-DI B-PEESCATI0001W5), active as of 24 Oct 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 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-PEESCATI0001W5 Basic UDI-DI D-PEESCATI0001W5UDI-DIDate2 Oct 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Device name
Frenodiar 10 buste
Model / reference
Catridal 10 buste, PEESCATI0001
Primary DI / UDI-DI
D-PEESCATI0001W5
Basic UDI-DI
B-PEESCATI0001W5
EMDN code
G0401 Orally administered devices for the therapy of gastro-intestinal disorders
Device class
Class IIa
EU registration type
Legacy device (under a directive)
EU market of registration
Spain

Manufacturer details

EUDAMED SRN
IT-MF-000032122

Similar devices in this category

Other devices filed under ORALLY ADMINISTERED DEVICES FOR THE THERAPY OF GASTRO-INTESTINAL DISORDERS.

Other devices from PHARMA LINE Srl

See all devices from PHARMA LINE Srl →

Properties

Other properties (12, all answered No)