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Netcell©

by Network Medical Products Limited

Ref 37-420Model PVA Wick and Wipe

Netcell© (37-420) is a Class I device made by Network Medical Products, Ltd., registered in EUDAMED on 5 Nov 2026 (Basic UDI-DI B-05060165018994), 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-05060165018994 Basic UDI-DI 05060165018994UDI-DIDate5 Nov 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Device name
PVA and Cellulose Ophthalmic (sterile, patient contacting)
Model / reference
PVA Wick and Wipe, 37-420
Primary DI / UDI-DI
05060165018994
Basic UDI-DI
B-05060165018994
EMDN code
Q0299 Ophthalmic devices - other
Device class
Class I
EU registration type
Legacy device (under a directive)
EU market of registration
Malta

Manufacturer details

EUDAMED SRN
GB-MF-000025518
Authorised representative
Advena Limited MT-AR-000000234

Other devices from Network Medical Products, Ltd.

See all devices from Network Medical Products, Ltd. →

Properties

  • Supplied sterile
Other properties (11, all answered No)