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EUDAMED last updated this device on Dec 17, 2025
0190302A49944TYSeqStudio™ 8 Flex Dx Capillary Array 50 cm is an EU IVDR-regulated in vitro diagnostic registered in EUDAMED. It is classified as IVDR Class A. Manufactured by Life Technologies Holdings Pte Ltd. Placed on the EU market in Netherlands. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
10190302015714A49944SG-MF-000023931(01)10190302015714
The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
Sterile
A sterile device is supplied free of viable micro-organisms — flagged so that it is handled, stored and used to preserve that sterile state.
Single-use device
A single-use device is intended to be used on one patient during a single procedure and then discarded — not reprocessed or reused.
Primary placement in Netherlands; available across 1 country total.
Placed on the market in Netherlands; per-country availability dates not published.
European Medical Device Nomenclature — the EU product classification assigned to this device.
W02050185NUCLEIC ACID TESTING INSTRUMENTS EXCEPT MICRO-ARRAYS - CONSUMABLESPrimary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
View in glossary →UDI issuing entities
Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.
View in glossary →IVDR risk classes
IVDR risk classes rank in-vitro diagnostic devices from lowest risk (Class A) to highest (Class D), based on the patient and public-health risk of a wrong result.
View in glossary →Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →No certificate specifically references this device's Basic UDI-DI.
No certificates registered for this manufacturer.
No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.0190302TCF0000576CAPOn the marketSepta Cathode Buffer Container Dx019030244107169TOn the marketSeqStudio™ 24 Flex Dx Capillary Array 50 cm0190302A49944TYOn the marketSeqStudio™ Flex Dx series 96-Well Fast (0.1 mL) Retainer & Base Set0190302A55961TFOn the marketSeqStudio™ Flex Dx series 96-Well Standard Retainer & Base Set0190302A55961TFOn the marketSequencing Standard BigDye™ Terminator v1.1 Dx01903024462113AUOn the market