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Virudet+

EUDAMED

Class I (EU MDR)

Ref J70FModel VDF

by Amity Limited

Identity

Trade Name
Virudet+ EUDAMED
Device Name
VDF EUDAMED
Model / Reference
VDF EUDAMED
J70F EUDAMED

Identifiers

Primary DI / UDI-DI
05060722250836 EUDAMED
Basic UDI-DI
506072225AAA0014JT EUDAMED
Direct Marketing DI
05060722250836 EUDAMED
EMDN Code
D0899 DETERGENTS FOR MEDICAL DEVICES - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Northern Ireland EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Virudet+ by Amity Limited — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Amity Limited
EUDAMED SRN
GB-MF-000023321
Authorised Representative
Amity Healthcare EU Ltd. IE-AR-000011613

Sources (2)

  • EUDAMED b82bdc75-ec02-4f43-a4aa-cf05326fd62f 61 fields · synced Jun 18, 2026
  • EUDAMED 75dcf8d1-2bcf-4176-b69c-bb46cae86696 61 fields · synced Jun 18, 2026