Taiwan FDA registration e5466cf9a5ba127809af27f81320bc34
"Arthur Come" nerve stimulation electrode patch
TW: “亞瑟康”神經刺激電極貼片
Taiwan·Risk Class 2·AXELGAARD MANUFACTURING CO., LTD.·Registered May 14, 2018 – May 23, 2028ActiveRegistration details
- Analysis ID
- e5466cf9a5ba127809af27f81320bc34
- Customs Code
- DHA00601886603
Company information
- Manufacturer
- AXELGAARD MANUFACTURING CO., LTD.
- Manufacturer Country
- United States
- Authorized Representative
- K&C MEDICAL CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- K Neuroscience
- Product Type (Level 2)
- K.1320 Skin electrode
- Import Information
- import
Dates and status
- Registration Date
- May 14, 2018
- Expiry Date
- May 23, 2028
About this record
Access comprehensive regulatory information for "Arthur Come" nerve stimulation electrode patch in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e5466cf9a5ba127809af27f81320bc34 and manufactured by AXELGAARD MANUFACTURING CO., LTD.. The authorized representative in Taiwan is K&C MEDICAL 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