Taiwan FDA registration f40077909e0cb18bf69cb6a051974212
"Wecon" limb equipment (unsterilized)
TW: “瑋肯” 肢體裝具(未滅菌)
Registration details
- Analysis ID
- f40077909e0cb18bf69cb6a051974212
Company information
- Manufacturer
- Aimin Eisai Co., Ltd. Plant 2
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- WEKEN MEDICAL INSTRUMENTS CO., LTD.
Product details
- Intended Use
- Limited to the first level recognition range of limb equipment (O.3475) of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- o Physical Medical Sciences
- Product Type (Level 2)
- O.3475 Limb fittings
- Import Information
- Domestic;; Contract manufacturing
Dates and status
- Registration Date
- Jan 21, 2011
- Expiry Date
- Jan 21, 2016
- 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 "Wecon" limb equipment (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f40077909e0cb18bf69cb6a051974212 and manufactured by Aimin Eisai Co., Ltd. Plant 2. The authorized representative in Taiwan is WEKEN MEDICAL INSTRUMENTS 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