Taiwan FDA registration 71c4bb9441489fbc56af5e37e7ea7893
"GeneHwa" Enzyme preparations (Non-Sterile)
TW: "菁驊" 酵素製劑 (未滅菌)
Taiwan·Risk Class 1·MD·DNA GENOTEK INC.·Registered Apr 23, 2018 – Apr 23, 2023ExpiredRegistration details
- Analysis ID
- 71c4bb9441489fbc56af5e37e7ea7893
- License Form
- Ministry of Health Medical Device Import No. 018995
- Customs Code
- DHA09401899501
Company information
- Manufacturer
- DNA GENOTEK INC.
- Manufacturer Country
- Canada
- Authorized Representative
- Jinghua Limited
Product details
- Intended Use
- Limited to the first level identification range of enzyme treatment reagents (B.4400) of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- B Hematology and pathology devices
- Product Type (Level 2)
- B4400 Enzyme Treatment Reagent
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Apr 23, 2018
- Expiry Date
- Apr 23, 2023
About this record
Access comprehensive regulatory information for "GeneHwa" Enzyme preparations (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 71c4bb9441489fbc56af5e37e7ea7893 and manufactured by DNA GENOTEK INC.. The authorized representative in Taiwan is Jinghua Limited.
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