Eu Ivdd
Eu Ivd General
On The Market
🇨🇳 China
Preimplantation Genetic Testing For Aneuploidy Detection Kit（Single Molecule Direct Sequencing）
Devices (same UDI-DI)
1
Certificates
0
Countries
0
Notified Bodies
0
Basic Information
- Primary DI
- 06974968583100
- Basic UDI-DI Code
- B-06974968583100
- Reference
- L000030
- Device Types
- None provided
- Regulation
- Eu Ivdd
- Classification
- Eu Ivd General
- Status
- On The Market
- Manufacturer
- GeneMind Biosciences Co., Ltd.
Additional Description
At present, chromosomal aneuploidy is the main cause of abortion and pregnancy failure in IVF. The results of preimplantation embryo chromosomal aneuploidy test (PGT-A) can assist clinicians in selecting embryos with normal chromosomes for implantation, thereby improving IVF Infant clinical pregnancy rate, reduce miscarriage rate, improve singleton implantation success rate, and avoid high risk caused by multiple birth implantation.
CND Nomenclature Codes
| Code | Description |
|---|---|
| W0106010399 | CHROMOSOMAL DISORDERS TESTS - OTHER |
Similar Devices
Other on-the-market devices with the same classification (Eu Ivd General) and regulation (EU IVDD).
BluBox
Device
EU IVDD
·
Eu Ivd General
·Blusense Diagnostics ApS·On the market·5 countries
extendSURE™ HbA1c Liquid Controls
Device
EU IVDD
·
Eu Ivd General
·Canterbury Scientific Limited·On the market·19 countries
ViroTrack Sero COVID-19 Total Ab
Device
EU IVDD
·
Eu Ivd General
·Blusense Diagnostics ApS·On the market·5 countries
extendSURETM Haemoglobin F and A2 Calibrators
Device
EU IVDD
·
Eu Ivd General
·Canterbury Scientific Limited·On the market·8 countries
extendSURE™ Haemoglobin F and A2 Controls
Device
EU IVDD
·
Eu Ivd General
·Canterbury Scientific Limited·On the market·8 countries
extendSURE™ HbA1c Liquid Controls
Device
EU IVDD
·
Eu Ivd General
·Canterbury Scientific Limited·On the market·19 countries