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RapidFor™Estradiol (E2) Rapid Test Kit (FIA)

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

Basic Information

Primary DI
08683548250810
Basic UDI-DI Code
B-08683548250810
Reference
VMPO43
Device Types
Single use
Regulation
Eu Ivdd
Classification
Eu Ivd General
Status
On The Market

Additional Description

This kit is suitable for in vitro quantitative detection of the concentration of Estradiol (E2) in human serum, plasma or whole blood. This product is used for testing in medical and health institutions for the auxiliary diagnosis of ovarian function.

CND Nomenclature Codes

Code Description
W0102050103 ESTRADIOL

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