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Viscoflu

by PHARMA LINE Srl 2 variants

Ref PEEVISC0001Model 10 vials model

Viscoflu (PEEVISC0001) is a Class IIb device made by PHARMA LINE Srl, registered in EUDAMED on 18 May 2026 (Basic UDI-DI 805826596FT006MDRRS), active as of 23 Oct 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number805826596FT006MDRRS Basic UDI-DI 08058265962405UDI-DIDate18 May 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Model / reference
10 vials model, PEEVISC0001
Primary DI / UDI-DI
08058265962405
Basic UDI-DI
805826596FT006MDRRS
EMDN code
R9099 Respiratory and anaesthesia devices - other
Device class
Class IIb
EU registration type
Standard device
EU market of registration
Estonia

Manufacturer details

EUDAMED SRN
IT-MF-000032122

Similar devices in this category

Other devices filed under RESPIRATORY AND ANAESTHESIA DEVICES - OTHER.

Other devices from PHARMA LINE Srl

See all devices from PHARMA LINE Srl →

Properties

  • Supplied sterile
Other properties (13, all answered No)