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QuantStudio™ 5 Dx Real‑Time PCR Instrument (96-Well 0.2ml Block)

EUDAMEDFDA UDI

Class A (EU MDR)

Ref A47324 (A47326, A47327)

by Life Technologies Holdings Pte Ltd

Identity

Trade Name
QuantStudio™ 5 Dx Real‑Time PCR Instrument (96-Well 0.2ml Block) EUDAMED
Applied Biosystems™ QuantStudio™ 5 Dx Real-Time PCR System FDA UDI
Generic Name
Thermal cycler nucleic acid amplification analyser IVD, laboratory FDA UDI
Device Name
QuantStudio™ 5 Dx Real-Time PCR System and Accessories EUDAMED
Model / Reference
A47324 (A47326, A47327) EUDAMED
A47324 FDA UDI

Identifiers

Primary DI / UDI-DI
10190302015592 EUDAMEDFDA UDI
Basic UDI-DI
0190302A47326SJ EUDAMED
FDA Product Code
OOI FDA UDI
EMDN Code
W02050116 NUCLEIC ACID TESTING INTEGRATED EXTRACTION /AMPLIFICATION /DETECTION SYSTEMS EUDAMED
GMDN Term
Thermal cycler nucleic acid amplification analyser IVD, laboratory FDA UDI

Classification

Device Class
Class A EUDAMED
Class II FDA UDI
Regulation Number
862.2570 FDA UDI
Market of Registration
Netherlands EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

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

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Nucleic acid sample preparation instrument IVD

QuantStudio™ 5 Dx Real‑Time PCR Instrument (96-Well 0.2ml Block) by Life Technologies Holdings Pte Ltd. — Class A — IVDR, FDA UDI — listed in EUDAMED, FDA GUDID

Similar devices

Also classified as Nucleic acid sample preparation instrument IVD.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/IVDR

United States Pending data

FDA UDI

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Manufacturer

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

Sources (3)

  • EUDAMED 5cec37fd-09a7-439f-aa3a-819615d05661 61 fields · synced Jun 19, 2026
  • FDA UDI f5b32caa-dd67-4fb2-bf04-60fcbd85a15e 32 fields · synced May 30, 2026
  • EUDAMED 5cec37fd-09a7-439f-aa3a-819615d05661-1 61 fields · synced Jun 9, 2026