Taiwan FDA registration 55cf6dfe85f92b7e3d3bd273b182da2d

Fujifilm measures the concentration of sodium, potassium and chlorine in blood as a dry test piece

TW: 富士測定血中鈉、鉀、氯濃度乾式試片
Taiwan flagTaiwan·Risk Class 2·FUJIFILM Healthcare Manufacturing Corporation Minamiashigara Nakanuma Office·Registered Jun 17, 2010 – Jun 17, 2025Expired
Registration details
Analysis ID
55cf6dfe85f92b7e3d3bd273b182da2d
Customs Code
DHA00602123007
Company information
Manufacturer Country
Japan
Authorized Representative
HUNG CHONG CORP.
Product details
Intended Use
The potential difference method is used to determine the concentration of sodium, potassium and chloride ions in whole blood, plasma or serum. In vitro diagnostic use.
Product Type (Level 1)
A Clinical chemistry and clinical toxicology
Product Type (Level 2)
A.1665 Sodium Test System
Import Information
import
Dates and status
Registration Date
Jun 17, 2010
Expiry Date
Jun 17, 2025
About this record

Access comprehensive regulatory information for Fujifilm measures the concentration of sodium, potassium and chlorine in blood as a dry test piece in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 55cf6dfe85f92b7e3d3bd273b182da2d and manufactured by FUJIFILM Healthcare Manufacturing Corporation Minamiashigara Nakanuma Office. The authorized representative in Taiwan is HUNG CHONG CORP..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

Free DatabasePowered by Pure Global AI89,000+ Devices