Diagnostic Kit for PRL (Time-resolved Fluorescence Immunochromatographic Assay)
Let the assistant research this device
The Research Assistant compiles risk class, certificates, notified bodies and related records — and cites every one.
Free to try · every answer cites its records
Basic Information
- Primary DI
- 06974521000693
- Basic UDI-DI Code
- B-06974521000693
- Reference
- SUPF045025
- Device Types
-
Single use
- Regulation
- Eu Ivdd
- Classification
- Eu Ivd General
- Status
- On The Market
- Manufacturer
- Shenzhen Superbio Technology Co.,Ltd.
Additional Description
This kit is suitable for in vitro quantitative detection of the concentration of prolactin (PRL) in human serum, plasma and whole blood samples. The main physiological function of prolactin is to stimulate and maintain female lactation. Pregnancy, sexual intercourse, breast stimulation, sleep, exercise, stress, estrogen, progesterone and some psychoactive drugs can increase prolactin levels. Taking bromocriptine, VitB6, and levodopa drugs can reduce prolactin levels. High levels of prolactin inhibit ovulation, which is also the main cause of female infertility and reproductive diseases.
CND Nomenclature Codes
| Code | Description |
|---|---|
| W0102050108 | PROLACTIN |
Similar Devices
Other on-the-market devices with the same classification (Eu Ivd General) and regulation (EU IVDD).