Taiwan FDA registration 6767237f3de49a3e1e8131f199d54378
"Ti-Ho" hematocrit centrifuge (Non-Sterile)
TW: "鈦和" 血球容積測量離心機 (未滅菌)
Registration details
- Analysis ID
- 6767237f3de49a3e1e8131f199d54378
- License Form
- Ministry of Health Medical Device Manufacturing No. 006646
Company information
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Titanium and Health Technology Co., Ltd. Zhonghe plant
Product details
- Intended Use
- Limited to the first level identification range of the blood cell volume measurement device (B.6400) of the medical equipment management method.
- Product Type (Level 1)
- B Hematology and pathology devices
- Product Type (Level 2)
- B6400 Blood cell volume measurement device
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Mar 21, 2017
- Expiry Date
- Mar 21, 2022
About this record
Access comprehensive regulatory information for "Ti-Ho" hematocrit centrifuge (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 6767237f3de49a3e1e8131f199d54378 and manufactured by Titanium and Health Technology Co., Ltd. Zhonghe plant. The authorized representative in Taiwan is Titanium and Health Technology Co., Ltd. Zhonghe plant.
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