Eu Ivdd Eu Ivd General On The Market 🇨🇳 China

AMH Assay kit CLIA

Devices (same UDI-DI)
1
Certificates
0
Countries
0
Notified Bodies
0

Basic Information

Primary DI
06974521001027
Basic UDI-DI Code
B-06974521001027
Reference
SUPM080072
Device Types
Single use
Regulation
Eu Ivdd
Classification
Eu Ivd General
Status
On The Market

Additional Description

This kit is used for in vitro quantitative detection of Anti-Mullerian Hormone (AMH) in human serum and (or) plasma. AMH is secreted by the supportive cells of the testis in men. In male embryonic development, AMH secretion by testicular supporting cells is responsible for the decline of the mullerian canal and the normal development of the male reproductive tract. AMH continues to develop from the testicles until puberty, and then slowly decreases to a post-pubertal level. In women, AMH plays an important role in ovarian follicular development. AMH is almost undetectable at new birth in women, which reaches its highest level after puberty, then gradually declines with age and becomes undetectable after menopause. The AMH test is clinically used to assess ovarian reserve to reflect the number of preantral follicle and to predict the response to controlled ovulation.

CND Nomenclature Codes

Code Description
W0102050215 ANTI-MÛLLERIAN HORMONE

Similar Devices

Other on-the-market devices with the same classification (Eu Ivd General) and regulation (EU IVDD).

View all