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PixoTest Capillary blood collection tube (Non-sterile) - Taiwan Registration 5ac57100682f20f74a44d1984f80967d

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..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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5ac57100682f20f74a44d1984f80967d
Registration Details
Taiwan FDA Registration: 5ac57100682f20f74a44d1984f80967d
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Device Details

PixoTest Capillary blood collection tube (Non-sterile)
TW: ๅฎ‰ๅฟ…ๆธฌๆฏ›็ดฐ็ฎก่ก€ๆถฒๆ”ถ้›†็ฎก (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

5ac57100682f20f74a44d1984f80967d

Ministry of Health Medical Device Manufacturing No. 008188

Company Information

Taiwan, Province of China

Product Details

Limited to the first level identification range of "Capillary Blood Collection Tube (B.6150)" under the Measures for the Administration of Medical Devices.

B Hematology and pathology devices

B6150 Capillary blood collection tube

Produced in Taiwan, China

Dates and Status

Feb 12, 2020

Feb 12, 2025