Taiwan FDA registration 71c1d7c660b9ccbe9e389cfc0eebedb8

Fujifilm - Dry test piece for measuring blood calcium concentration

TW: 富士-測定血鈣濃度乾式試片

Taiwan·Risk Class 2·FUJIFILM Healthcare Manufacturing Corporation Minamiashigara Nakanuma Office·Registered Jan 26, 2006 – Jan 26, 2026Expired

Registration details

Analysis ID: 71c1d7c660b9ccbe9e389cfc0eebedb8
Customs Code: DHA00601595602

Company information

Manufacturer: FUJIFILM Healthcare Manufacturing Corporation Minamiashigara Nakanuma Office
Manufacturer Country: Japan
Authorized Representative: HUNG CHONG CORP.

Product details

Intended Use: The total concentration of calcium in serum and plasma is measured.
Product Type (Level 1): A Clinical chemistry and clinical toxicology
Product Type (Level 2): A.1145 Calcium Test System
Import Information: import

Dates and status

Registration Date: Jan 26, 2006
Expiry Date: Jan 26, 2026

About this record

Access comprehensive regulatory information for Fujifilm - Dry test piece for measuring blood calcium concentration in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 71c1d7c660b9ccbe9e389cfc0eebedb8 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.