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Banduff

EUDAMED

Class I (EU MDR)

Ref UF8050

by Honnes Sağlık ve Endüstriyel Ürünleri A.Ş

Identity

Trade Name
Banduff EUDAMED
Device Name
Aid Plaster EUDAMED
Model / Reference
UF8050 EUDAMED

Identifiers

Primary DI / UDI-DI
08681285103000 EUDAMED
Basic UDI-DI
868128510BF10032Y EUDAMED
EMDN Code
M0599 MEDICAL PLASTERS - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Austria 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

Banduff by Honnes Sağlık ve Endüstriyel Ürünleri A.Ş — 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

EUDAMED SRN
TR-MF-000017199

Sources (1)

  • EUDAMED 6c6278b2-be0a-4498-a94a-cd5bbb095467 61 fields · synced Oct 5, 2026