7933162

Organization name

Genome Diagnostics B.V.

SRN

NL-MF-000000453

Manufacturer status

Active

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• CW010

  Consult instructions for use before use

Primary placement in Netherlands; available across 32 countries total.

Trade name

not provided

UDI-DI code

08718469366712

Basic UDI-DI

871846936ngsgo-ampxv3F6

Reference / catalog number

7933162

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

NGSgo-AmpX v3 are qualitative in vitro diagnostic kits, intended for the amplification of the following genes in human genomic DNA specimens: - HLA Class I: HLA-A, HLA-B, HLA-C - HLA Class II: HLA-DRB1, HLA-DRB3, HLA-DRB4, HLA-DRB5, HLA DQA1, HLA DQB1, HLA-DPA1, HLA DPB1 The kit is intended to generate HLA amplicons by PCR (polymerase chain reaction), which are suitable for HLA genotyping at high-resolution level. The generated amplicons can be used as input for downstream Next-Generation Sequencing (NGS) applications. It is a single-use, non-automated assay to aid in the diagnosis of HLA gene compatibility between donor and recipient for transplantation purposes (e.g. hematopoietic stem cell transplantation). The intended testing population are both, transplant donors as well as transplant recipients. NGSgo-AmpX v3 is intended for laboratory professional use in an EFI or ASHI accredited diagnostic laboratory setting, by personnel trained in PCR amplification. It is intended to be used for transplantation procedures where time is not a critical factor.

Additional information URL

https://www.gendx.com/ifu2/

Clinical sizes

No clinical sizes registered for this device.

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• Expiration date
• Manufacturing date
• Serial number
• Software identification

European Medical Device Nomenclature — the EU product classification assigned to this device.

• W01030499TISSUE TYPING REAGENTS - OTHER