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“Applied” Voyant Fine Fusion Device - Taiwan Registration 9af511eac4b6cfac87c2dd6ec16c9c33

Access comprehensive regulatory information for “Applied” Voyant Fine Fusion Device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9af511eac4b6cfac87c2dd6ec16c9c33 and manufactured by APPLIED MEDICAL RESOURCES CORPORATION. The authorized representative in Taiwan is DOUBLE-SUCCESS CO., 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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9af511eac4b6cfac87c2dd6ec16c9c33
Registration Details
Taiwan FDA Registration: 9af511eac4b6cfac87c2dd6ec16c9c33
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Device Details

“Applied” Voyant Fine Fusion Device
TW: “安培”精細式組織凝結刀
Risk Class 2
MD

Registration Details

9af511eac4b6cfac87c2dd6ec16c9c33

Ministry of Health Medical Device Import No. 036020

DHA05603602007

Company Information

United States

Product Details

Details are as detailed as approved Chinese instructions

I General, Plastic Surgery and Dermatology

I4400 Electric knife for cutting and hemostasis and its accessories

Imported from abroad

Dates and Status

Oct 31, 2022

Oct 31, 2027