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Qvintip

EUDAMED

Class A (EU MDR)

Ref 10-012Ref 10-002

by Aprovix AB

Identity

Trade Name
Qvintip EUDAMED
Device Name
Qvintip Sampling Kit EUDAMED
Qvintip Sampler EUDAMED
Model / Reference
10-012 EUDAMED
10-002 EUDAMED

Identifiers

Primary DI / UDI-DI
07350187090039 EUDAMED
07350187090022 EUDAMED
Basic UDI-DI
73501870910-012EG EUDAMED
73501870910-002ED EUDAMED
EMDN Code
A1101 SAMPLE COLLECTION NEUTRAL SWABS EUDAMED

Classification

Device Class
Class A EUDAMED
Class I EUDAMED
Market of Registration
Sweden 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

Microbial Substances

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Reagent

No

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

No

EUDAMED

Companion Diagnostics

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Surgical Instrument

No

EUDAMED

New Device

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Category: General-purpose absorbent tip applicator/swab, single-use

Qvintip by Aprovix AB — Class A — MDR, IVDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as General-purpose absorbent tip applicator/swab, single-use.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

European Union Active

CE/IVDR

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Manufacturer

Manufacturer
Aprovix AB
EUDAMED SRN
SE-MF-000048905

Sources (2)

  • EUDAMED e8ecf0f3-d281-45c3-ba7c-2ab51794fab8 61 fields · synced Jul 26, 2026
  • EUDAMED dfea7064-65ad-47e8-8826-4e8303595bcb 61 fields · synced May 19, 2026