Eu Ivdd Eu Ivd General On The Market 🇹🇷 Türkiye

RapidFor™ FSH Rapid Test Kit (FIA)

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

Basic Information

Primary DI
08683548250506
Basic UDI-DI Code
B-08683548250506
Reference
VMPO39
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 Follicle Stimulating Hormone (FSH) in human serum, plasma or whole blood samples.

CND Nomenclature Codes

Code Description
W0102050104 FOLLICLE STIMULATING HORMONE

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