Taiwan FDA registration 42d58cfd5f9b4f0d9196ef31f1aa8696
"Nates" Teika disposable coaxial needle electrode
TW: “納特斯”泰卡拋棄式同軸針狀電極
Taiwan·Risk Class 2·Natus Manufacturing Ltd.·Registered May 24, 2013 – May 24, 2028ActiveRegistration details
- Analysis ID
- 42d58cfd5f9b4f0d9196ef31f1aa8696
- Customs Code
- DHA00602495501
Company information
- Manufacturer
- Natus Manufacturing Ltd.
- Manufacturer Country
- Ireland
- Authorized Representative
- SYNGROWTH CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- o Physical Medical Sciences
- Product Type (Level 2)
- O.1385 診斷用肌電圖針電極
- Import Information
- Input;; Contract manufacturing
Dates and status
- Registration Date
- May 24, 2013
- Expiry Date
- May 24, 2028
About this record
Access comprehensive regulatory information for "Nates" Teika disposable coaxial needle electrode in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 42d58cfd5f9b4f0d9196ef31f1aa8696 and manufactured by Natus Manufacturing Ltd.. The authorized representative in Taiwan is SYNGROWTH 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