Taiwan FDA registration 4eb20cb0cf1544119dabc486db9efa91

"Titanium subfamily" double-frame cell calculation disk (unsterilized)

TW: "鈦亞科" 雙畫格細胞計算盤 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·AVE SCIENCE & TECHNOLOGY CO., LTD.·Registered Aug 14, 2019 – Aug 14, 2024Expired
Registration details
Analysis ID
4eb20cb0cf1544119dabc486db9efa91
Customs Code
DHA09600392201
Company information
Manufacturer Country
China
Authorized Representative
DiaTech Technology Co., Ltd.
Product details
Intended Use
It is limited to the first level of identification of the "Manual Blood Cell Counting Device (B.6160)" of the Administrative Measures for the Classification and Grading of Medical Devices.
Product Type (Level 1)
B Hematology, pathology, and genetics
Product Type (Level 2)
B.6160 Hand haemocytometry numerals
Import Information
Input;; Chinese goods
Dates and status
Registration Date
Aug 14, 2019
Expiry Date
Aug 14, 2024
About this record

Access comprehensive regulatory information for "Titanium subfamily" double-frame cell calculation disk (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 4eb20cb0cf1544119dabc486db9efa91 and manufactured by AVE SCIENCE & TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is DiaTech Technology 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.

Free DatabasePowered by Pure Global AI89,000+ Devices