Skip to content

Vismed®

by TRB Chemedica AG 8 variants

Part of a family of 10 devices: see the family page

Ref 04028694000331

Vismed® (04028694000331) is a Class IIb device made by TRB Chemedica AG, registered in EUDAMED on 7 Aug 2025 (Basic UDI-DI 4028694VISMED3F), 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 Number4028694VISMED3F Basic UDI-DI 04028694000331UDI-DIDate7 Aug 2025RegisteredStatusActive EUDAMED: not on the EU market

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device name
Vismed®
Model / reference
04028694000331
Primary DI / UDI-DI
04028694000331
Basic UDI-DI
4028694VISMED3F
EMDN code
Q02030301 Ophthalmology, hyaluronic acid and derivatives
Device class
Class IIb
EU registration type
Standard device

Manufacturer details

EUDAMED SRN
DE-MF-000006919

Similar devices in this category

Other devices filed under OPHTHALMOLOGY, HYALURONIC ACID AND DERIVATIVES.

Other devices from TRB Chemedica AG

See all devices from TRB Chemedica AG →

Properties

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