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Q-Pad Kit

EUDAMED

Class I (EU MDR)

Ref QD1.3Model Q-Pad Kit

by Qurasense, Inc.

Identity

Trade Name
Q-Pad Kit EUDAMED
Device Name
Q-Pad Kit EUDAMED
Model / Reference
Q-Pad Kit EUDAMED
QD1.3 EUDAMED

Identifiers

Primary DI / UDI-DI
00860004423478 EUDAMED
Basic UDI-DI
008600044234QPAD79 EUDAMED
EMDN Code
A99 DEVICES FOR ADMINISTRATION, WITHDRAWAL AND COLLECTION - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Denmark 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

Q-Pad Kit by Qurasense, Inc. — 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
Qurasense, Inc.
EUDAMED SRN
US-MF-000052772
Authorised Representative
Specculo Limited MT-AR-000034988

Sources (1)

  • EUDAMED fc38e2ad-0118-4fd2-b7db-e1e243da8a3d 61 fields · synced Jun 19, 2026