Eu Ivdd Eu Ivd General On The Market 🇨🇳 China

Pepsinogen Ⅰ(PGⅠ)Assay Kit

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

Basic Information

Primary DI
06954376005517
Basic UDI-DI Code
B-06954376005517
Reference
69543760F000696V
Device Types
None provided
Regulation
Eu Ivdd
Classification
Eu Ivd General
Status
On The Market

Additional Description

This kit is intended for in vitro quantitative detection of Pepsinogen I (PG I) in human serum. Clinically, this kit is available to monitor PG I concentration and PG I/II ratio. It is used for treatment monitoring of gastric cancer, but not for tumor screening in the general population.

CND Nomenclature Codes

Code Description
W0102069006 PEPSINOGEN

Similar Devices

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

View all