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Qlicksmart BladeFLASK

EUDAMED

Class I (EU MDR)

Ref QFYGENModel Qlicksmart Scalpel Blade Remover

by Qlicksmart Pty Ltd

Identity

Trade Name
Qlicksmart BladeFLASK EUDAMED
Device Name
Qlicksmart Scalpel Blade Remover EUDAMED
Model / Reference
Qlicksmart Scalpel Blade Remover EUDAMED
QFYGEN EUDAMED

Identifiers

Primary DI / UDI-DI
09337363001247 EUDAMED
Basic UDI-DI
93373630QSBRFL00001PQ EUDAMED
EMDN Code
V0499,V9099 EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Netherlands 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

Qlicksmart BladeFLASK by Qlicksmart Pty Ltd — 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
Qlicksmart Pty Ltd
EUDAMED SRN
AU-MF-000033870
Authorised Representative
Donawa Lifescience Consulting Srl IT-AR-000007785

Sources (1)

  • EUDAMED 3f6156b6-4d4b-48aa-9db1-dcdb5adf10d0 61 fields · synced May 25, 2026