"Medtronic" Eti neurostimulator
- Analysis ID
- 8530b6b12fd5aba11ae12a53edd5bb47
- Customs Code
- DHA00602337606
- Manufacturer Country
- United States
- Authorized Representative
- MEDTRONIC (TAIWAN) LTD.
- Intended Use
- Details are Chinese Generic Approved Version;102.10.8. Performance Changes: Details as Chinese Generic Approved Version, the following blanks.103.5.26. Performance Changes: Details as Chinese Generic Approved Version, the following blanks.
- Product Type (Level 1)
- K Neuroscience
- Import Information
- Safety monitoring;; import
- Registration Date
- Mar 16, 2012
- Expiry Date
- Mar 16, 2027
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Access comprehensive regulatory information for "Medtronic" Eti neurostimulator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 8530b6b12fd5aba11ae12a53edd5bb47 and manufactured by Medtronic Puerto Rico Operations Co., Juncos;; Medtronic Inc.. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including Medtronic Inc.;; MEDTRONIC PUERTO RICO OPERATIONS CO., VILLALBA, MEDTRONIC NEUROMODULATION;; Medtronic Inc., and 2 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.