Taiwan FDA registration 98cf63a87e70b00798f89f637d3a381b
"Medtronic" test line
TW: “美敦力”思特測試纜線
Registration details
- Analysis ID
- 98cf63a87e70b00798f89f637d3a381b
- Customs Code
- DHA05603602504
Company information
- Manufacturer
- MEDTRONIC NEUROMODULATION;; Medtronic Inc.
- Manufacturer Country
- United States
- Authorized Representative
- MEDTRONIC (TAIWAN) LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- K Neuroscience
- Product Type (Level 2)
- K.9999 Miscellaneous
- Import Information
- import
Dates and status
- Registration Date
- Nov 02, 2022
- Expiry Date
- Nov 02, 2027
About this record
Access comprehensive regulatory information for "Medtronic" test line in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 98cf63a87e70b00798f89f637d3a381b and manufactured by MEDTRONIC NEUROMODULATION;; Medtronic Inc.. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) 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