← Back to catalogue

Applied Biosystems™ SeqStudio™ 24 Flex Dx Genetic Analyzer

EUDAMED

Class A (EU MDR)

Ref A50535

by Life Technologies Holdings Pte Ltd

Identity

Trade Name
Applied Biosystems™ SeqStudio™ 24 Flex Dx Genetic Analyzer EUDAMED
Device Name
Applied Biosystems™ SeqStudio™ Flex Dx Series Genetic Analyzer EUDAMED
Model / Reference
A50535 EUDAMED

Identifiers

Primary DI / UDI-DI
10190302018876 EUDAMED
Basic UDI-DI
0190302A50534RM EUDAMED
EMDN Code
W02050116 NUCLEIC ACID TESTING INTEGRATED EXTRACTION /AMPLIFICATION /DETECTION SYSTEMS EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Netherlands 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

Yes

EUDAMED

New Device

No

EUDAMED

Category: Nucleic acid sample preparation instrument IVD

Applied Biosystems™ SeqStudio™ 24 Flex Dx Genetic Analyzer by Life Technologies Holdings Pte Ltd. — Class A — IVDR — listed in EUDAMED

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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
SG-MF-000023931
Authorised Representative
Life Technologies Europe B.V. NL-AR-000021890

Sources (1)

  • EUDAMED 3214fef7-b75a-43d1-87f0-fa6562470f07 61 fields · synced Jun 19, 2026