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“MEGADYNE” ACE BLADE 700 - Taiwan Registration 48574b35e6cb783d7fb9d022e70c10b7

Access comprehensive regulatory information for “MEGADYNE” ACE BLADE 700 in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 48574b35e6cb783d7fb9d022e70c10b7 and manufactured by Megadyne Medical Products, Inc.. The authorized representative in Taiwan is JOHNSON & JOHNSON MEDICAL 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.

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48574b35e6cb783d7fb9d022e70c10b7
Registration Details
Taiwan FDA Registration: 48574b35e6cb783d7fb9d022e70c10b7
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Device Details

“MEGADYNE” ACE BLADE 700
TW: “美佳泰”王牌外科電刀筆
Risk Class 2
MD

Registration Details

48574b35e6cb783d7fb9d022e70c10b7

Ministry of Health Medical Device Import No. 033149

DHA05603314907

Company Information

United States

Product Details

For details, it is Chinese approved copy of the imitation order

I General and plastic surgical devices

I4400 Electric knife for cutting and hemostasis and its accessories

Imported from abroad

Dates and Status

Dec 30, 2019

Dec 30, 2024