Taiwan FDA registration d182d846fba0b232f4cc4db8dad5e5ff
FUJI DRI-CHEM CALIBRATOR CP(CRP)
TW: 富士校正液(C-反應蛋白)
Taiwan·Risk Class 2·MD·FUJIFILM Healthcare Manufacturing Corporation Minamiashigara Nakanuma Office·Registered Dec 17, 2013 – Dec 17, 2028ActiveRegistration details
- Analysis ID
- d182d846fba0b232f4cc4db8dad5e5ff
- License Form
- Ministry of Health Medical Device Import No. 025705
- Customs Code
- DHA05602570502
Company information
- Manufacturer Country
- Japan
- Authorized Representative
- HUNG CHONG CORP.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A1150 calibrate
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 17, 2013
- Expiry Date
- Dec 17, 2028
About this record
Access comprehensive regulatory information for FUJI DRI-CHEM CALIBRATOR CP(CRP) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d182d846fba0b232f4cc4db8dad5e5ff and manufactured by FUJIFILM Healthcare Manufacturing Corporation Minamiashigara Nakanuma Office. The authorized representative in Taiwan is HUNG CHONG CORP..
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