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isoQuarkF2

EUDAMED

Class A (EU MDR)

Ref RS-AIF2-E001

by RevoSketch Inc.

Identity

Trade Name
isoQuarkF2 EUDAMED
Device Name
isoQuarkF2 EUDAMED
Model / Reference
RS-AIF2-E001 EUDAMED

Identifiers

Primary DI / UDI-DI
08800122900002 EUDAMED
Basic UDI-DI
88001229AIF2J9 EUDAMED
Direct Marketing DI
08800122900002 EUDAMED
EMDN Code
W02050116 NUCLEIC ACID TESTING INTEGRATED EXTRACTION /AMPLIFICATION /DETECTION SYSTEMS EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Spain EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

No

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

New Device

No

EUDAMED

Category: Nucleic acid sample preparation instrument IVD

isoQuarkF2 by RevoSketch Inc. — Class A — IVDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Nucleic acid sample preparation instrument IVD.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

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Manufacturer

Manufacturer
RevoSketch Inc.
EUDAMED SRN
KR-MF-000037550
Authorised Representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Sources (1)

  • EUDAMED 0538a792-5f1c-4a99-897c-d2746d1f26f1 61 fields · synced Jun 20, 2026