Taiwan FDA registration 6ce27a4ab9883ed58d62ac54b9667692
“RHYTHMLINK” Disposable Single Subdermal Needle Electrodes
TW: “瑞斯林肯”拋棄式皮下針狀電極
Taiwan·Risk Class 2·MD·RHYTHMLINK INTERNATIONAL, LLC·Registered Oct 31, 2022 – Oct 31, 2027ActiveRegistration details
- Analysis ID
- 6ce27a4ab9883ed58d62ac54b9667692
- License Form
- Ministry of Health Medical Device Import No. 036022
- Customs Code
- DHA05603602201
Company information
- Manufacturer
- RHYTHMLINK INTERNATIONAL, LLC
- Manufacturer Country
- United States
- Authorized Representative
- WELLGROWTH TECHNOLOGY CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- K Neuroscience
- Product Type (Level 2)
- K1350 Needle Type Electrode
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 31, 2022
- Expiry Date
- Oct 31, 2027
About this record
Access comprehensive regulatory information for “RHYTHMLINK” Disposable Single Subdermal Needle Electrodes in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6ce27a4ab9883ed58d62ac54b9667692 and manufactured by RHYTHMLINK INTERNATIONAL, LLC. The authorized representative in Taiwan is WELLGROWTH 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