Taiwan FDA registration 71995cc3230078118df6d01587046249

Medtronic Cardiovascular Surgical Instruments (Sterilized)

TW: “美敦力”心臟血管外科器械 (滅菌)
Taiwan flagTaiwan·Risk Class 1·Medtronic Inc.;; MEDTRONIC PERFUSION SYSTEMS·Registered Oct 27, 2006 – Oct 27, 2026Active
Registration details
Analysis ID
71995cc3230078118df6d01587046249
Customs Code
DHA04400527403
Company information
Manufacturer Country
United States
Authorized Representative
MEDTRONIC (TAIWAN) LTD.
Product details
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
Dates and status
Registration Date
Oct 27, 2006
Expiry Date
Oct 27, 2026
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About this record

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.

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