Eu Ivdd Eu Ivd General On The Market 🇨🇳 China

PROG Rapid Quantitative Test

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

Basic Information

Primary DI
06933260208418
Basic UDI-DI Code
B-06933260208418
Reference
BT2203
Device Types
Single use
Regulation
Eu Ivdd
Classification
Eu Ivd General
Status
On The Market

Additional Description

The Biotime PROG (Progesterone) Rapid Quantitative Test is intended to quantify the concentration of PROG in human serum on Biotime FIA Analyzer by fluorescent immunoassay. The test is used as an aid detection of ovulation, the progesterone replacement therapy andhormone.

CND Nomenclature Codes

Code Description
W0102160399 FERTILITY/PREGNANCY RT & POC - OTHER

Similar Devices

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

View all