Medtronic Cardiovascular Surgical Instruments (Sterilized)
- Analysis ID
- 71995cc3230078118df6d01587046249
- Customs Code
- DHA04400527403
- Manufacturer
- Medtronic Inc.;; MEDTRONIC PERFUSION SYSTEMS
- Manufacturer Country
- United States
- Authorized Representative
- MEDTRONIC (TAIWAN) LTD.
- Intended Use
- Limited to the classification and grading management of medical equipment, the first level identification range of cardiovascular surgical instruments (E.4500).
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.4500 心臟血管外科器械
- Import Information
- Input;; QMS/QSD
- Registration Date
- Oct 27, 2006
- Expiry Date
- Oct 27, 2026
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Access comprehensive regulatory information for Medtronic Cardiovascular Surgical Instruments (Sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 71995cc3230078118df6d01587046249 and manufactured by Medtronic Inc.;; MEDTRONIC PERFUSION SYSTEMS. 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 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.