"Medtronic" extracorporeal neurostimulator
- Analysis ID
- 0b37c5abbd1fa854f86a6f30ee3dfa44
- Customs Code
- DHA05603087702
- Manufacturer
- MEDTRONIC NEUROMODULATION;; Medtronic Inc.
- Manufacturer Country
- United States
- Authorized Representative
- MEDTRONIC (TAIWAN) LTD.
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- K Neuroscience
- Product Type (Level 2)
- K.5880 Implantable spinal cord stimulator for pain relief
- Import Information
- import
- Registration Date
- Feb 12, 2018
- Expiry Date
- Feb 12, 2028
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Access comprehensive regulatory information for "Medtronic" extracorporeal neurostimulator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0b37c5abbd1fa854f86a6f30ee3dfa44 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, 1 companies making similar products including Medtronic Puerto Rico Operations Co., Juncos;; Medtronic Inc., and 1 recent registrations in the same category. 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.