Taiwan FDA registration 847a4b20e2c147dadbe1a21fbb7f8e9f
Fujifilm Assay Starch/Dry Test Piece
TW: 富士測定澱粉/乾式試片
Taiwan·Risk Class 2·FUJIFILM Healthcare Manufacturing Corporation Minamiashigara Nakanuma Office·Registered Feb 27, 2006 – Feb 27, 2026ExpiredRegistration details
- Analysis ID
- 847a4b20e2c147dadbe1a21fbb7f8e9f
- Customs Code
- DHA00601605903
Company information
- Manufacturer Country
- Japan
- Authorized Representative
- HUNG CHONG CORP.
Product details
- Intended Use
- Measure the concentration of starch in serum and plasma.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1070 澱粉酶試驗系統
- Import Information
- import
Dates and status
- Registration Date
- Feb 27, 2006
- Expiry Date
- Feb 27, 2026
About this record
Access comprehensive regulatory information for Fujifilm Assay Starch/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 847a4b20e2c147dadbe1a21fbb7f8e9f and manufactured by FUJIFILM Healthcare Manufacturing Corporation Minamiashigara Nakanuma Office. The authorized representative in Taiwan is HUNG CHONG CORP..
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