Taiwan FDA registration 5ac57100682f20f74a44d1984f80967d
PixoTest Capillary blood collection tube (Non-sterile)
TW: 安必測毛細管血液收集管 (未滅菌)
Taiwan·Risk Class 1·MD·Inner Lake Plant of AXA Shengke Co., Ltd·Registered Feb 12, 2020 – Feb 12, 2025ExpiredRegistration details
- Analysis ID
- 5ac57100682f20f74a44d1984f80967d
- License Form
- Ministry of Health Medical Device Manufacturing No. 008188
Company information
- Manufacturer
- Inner Lake Plant of AXA Shengke Co., Ltd
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- IXENSOR CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of "Capillary Blood Collection Tube (B.6150)" under the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- B Hematology and pathology devices
- Product Type (Level 2)
- B6150 Capillary blood collection tube
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Feb 12, 2020
- Expiry Date
- Feb 12, 2025
About this record
Access comprehensive regulatory information for PixoTest Capillary blood collection tube (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 5ac57100682f20f74a44d1984f80967d and manufactured by Inner Lake Plant of AXA Shengke Co., Ltd. The authorized representative in Taiwan is IXENSOR CO., LTD..
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