Taiwan FDA registration c9ed22de2900fe1261dce9e6251b9348

Fujifilm measures the concentration of urea nitrogen in blood with a dry test piece

TW: 富士測量血中尿素氮濃度乾式試片
Taiwan flagTaiwan·Risk Class 2·FUJIFILM Healthcare Manufacturing Corporation Minamiashigara Nakanuma Office·Registered Nov 23, 2010 – Nov 23, 2025Expired
Registration details
Analysis ID
c9ed22de2900fe1261dce9e6251b9348
Customs Code
DHA00602180802
Company information
Manufacturer Country
Japan
Authorized Representative
HUNG CHONG CORP.
Product details
Intended Use
WITH FUJI–CHEM ANALYZER TO MEASURE UREA NITROGEN CONCENTRATION IN PLASMA OR SERUM.
Product Type (Level 1)
A Clinical chemistry and clinical toxicology
Product Type (Level 2)
A.1770 尿素氮試驗系統
Import Information
import
Dates and status
Registration Date
Nov 23, 2010
Expiry Date
Nov 23, 2025
About this record

Access comprehensive regulatory information for Fujifilm measures the concentration of urea nitrogen in blood with 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 c9ed22de2900fe1261dce9e6251b9348 and manufactured by FUJIFILM Healthcare Manufacturing Corporation Minamiashigara Nakanuma Office. The authorized representative in Taiwan is HUNG CHONG CORP..

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