Taiwan FDA registration 8578e1bac07942030866b6deddef4ecb

Kaiwu Technology Mycobacterium tuberculosis detection kit

TW: 開物科技結核桿菌檢測試劑盒
Taiwan flagTaiwan·Risk Class 1·INTEC PRODUCTS, INC.·Registered Jun 09, 2010 – Jun 09, 2015Cancelled
Registration details
Analysis ID
8578e1bac07942030866b6deddef4ecb
Customs Code
DHA04600095202
Company information
Manufacturer Country
China
Product details
Intended Use
Limited to the first level identification range of Mycobacterium tuberculosis immunofluorescent reagent (C.3370) of the management method for medical devices.
Product Type (Level 1)
C Immunology and microbiology
Product Type (Level 2)
C.3370 結核桿菌免疫螢光試劑
Import Information
Input;; Chinese goods
Dates and status
Registration Date
Jun 09, 2010
Expiry Date
Jun 09, 2015
Cancellation Date
Jun 25, 2018
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
About this record

Access comprehensive regulatory information for Kaiwu Technology Mycobacterium tuberculosis detection kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 8578e1bac07942030866b6deddef4ecb and manufactured by INTEC PRODUCTS, INC.. The authorized representative in Taiwan is Kaiwu Technology Co., Ltd. Tainan Branch.

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