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GeneXpert®

EUDAMEDFDA UDI

Class A (EU MDR)

Ref GX-INFINITY 80

by Cepheid

Identity

Trade Name
GeneXpert® EUDAMEDFDA UDI
Generic Name
Thermal cycler nucleic acid amplification analyser IVD, laboratory FDA UDI
Device Name
GeneXpert® Infinity Systems EUDAMED
Xpert MTB/RIF Assay, GeneXpert Dx, GeneXpert Infinity-48, GeneXpert Infinity-48s, GeneXpert Infinity-80 FDA UDI
Model / Reference
GX-INFINITY 80 EUDAMEDFDA UDI
Description
Xpert MTB/RIF Assay, GeneXpert Dx, GeneXpert Infinity-48, GeneXpert Infinity-48s, GeneXpert Infinity-80 FDA UDI

Identifiers

Catalog Number
GX-INFINITY 80 FDA UDI
Primary DI / UDI-DI
07332940007720 EUDAMEDFDA UDI
Basic UDI-DI
081164701-INFINITY-ZH 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

Yes

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

Yes

EUDAMED

New Device

No

EUDAMED

Prescription Use

No

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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Nucleic acid sample preparation instrument IVD

GeneXpert® by Cepheid — Class A — IVDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

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

Manufacturer
Cepheid
EUDAMED SRN
US-MF-000010979
Authorised Representative
Cepheid AB SE-AR-000048904

Sources (2)

  • EUDAMED 8bab66fe-022c-4c2e-8b52-ff9fdcb106df 61 fields · synced Jul 10, 2026
  • FDA UDI 470614e9-4431-4f04-8b3b-c14081a33404 36 fields · synced May 30, 2026