Taiwan FDA registration afef713742feb7d27d8c91e971ea7d11

"Satoshi" Saliva Microovulation Microscopic Detector (Unsterilized)

TW: "聰運" 唾液微型排卵顯微鏡檢器 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·OMNIMATE ENTERPRISE CO., LTD.·Registered Mar 10, 2017 – Mar 10, 2022Cancelled
Registration details
Analysis ID
afef713742feb7d27d8c91e971ea7d11
Company information
Manufacturer Country
Taiwan, Province of China
Authorized Representative
TYI SYSTEMS LTD.
Product details
Intended Use
Limited to the first level recognition range of the "Luteinizing hormone test system (A.1485)" of the Measures for the Administration of Medical Devices.
Product Type (Level 1)
A Clinical chemistry and clinical toxicology
Product Type (Level 2)
A.1485 Progesterone testing system
Import Information
Domestic;; Contract manufacturing
Dates and status
Registration Date
Mar 10, 2017
Expiry Date
Mar 10, 2022
Cancellation Date
Apr 12, 2024
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
About this record

Access comprehensive regulatory information for "Satoshi" Saliva Microovulation Microscopic Detector (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number afef713742feb7d27d8c91e971ea7d11 and manufactured by OMNIMATE ENTERPRISE CO., LTD.. The authorized representative in Taiwan is TYI SYSTEMS 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