A58209

Organization name

GeneProof a.s.

SRN

CZ-MF-000002370

Manufacturer status

Active

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• CW010

  EUDAMED did not publish a description for this code.

Primary placement in Czechia; available across 2 countries total.

Trade name

not provided

UDI-DI code

08595696304102

Basic UDI-DI

859569630034QJ

Reference / catalog number

A58209

Issuing entity

GS1

Risk category

IVDR Class C

Applicable legislation

IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]

Status

On the market

Quantity

1

Additional product description

The intended purpose of the device is related to the medical context and clinical conditions under which the device may be used. Chlamydia pneumoniae infection is manifested by various symptoms such as cough, fever, headache, and malaise, or it can develop into laryngitis, pharyngitis, or pneumonia. Rarely, serious complications such as asthma exacerbation, encephalitis or myocarditis may occur. The GeneProof Chlamydia pneumoniae PCR Kit is an in vitro nucleic acid amplification test intended for qualitative detection of Chlamydia pneumoniae by real-time polymerase chain reaction (PCR) method. The clinical specimens used for detection are BAL, sputum and swab. The GeneProof Chlamydia pneumoniae PCR Kit can be used in combination with a manual or automated extraction system. The kit is designed for human in vitro diagnostics and provides qualitative detection. The kit is intended for diagnostics and aid to diagnosis, and it is designed for professional use in laboratories with trained staff.

Additional information URL

https://thermofisher.com/geneproofIFU

Clinical sizes

No clinical sizes registered for this device.

• W0105010118CHLAMYDIA PNEUMONIAE DETECTION BY NA REAGENTS

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• Expiration date
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