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“Cayenne” Biowick Surelock Implant - Taiwan Registration b295ad83b2806ad84ddd210ebcdb94f5

Access comprehensive regulatory information for “Cayenne” Biowick Surelock Implant in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b295ad83b2806ad84ddd210ebcdb94f5 and manufactured by Cayenne Medical, Inc.. The authorized representative in Taiwan is ZIMMER BIOMET TAIWAN 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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b295ad83b2806ad84ddd210ebcdb94f5
Registration Details
Taiwan FDA Registration: b295ad83b2806ad84ddd210ebcdb94f5
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Device Details

“Cayenne” Biowick Surelock Implant
TW: “凱燕”百威秀拉植入物
Risk Class 2
MD

Registration Details

b295ad83b2806ad84ddd210ebcdb94f5

Ministry of Health Medical Device Import No. 032861

DHA05603286107

Company Information

United States

Product Details

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

N Orthopedic devices

N3040 Smooth or threaded metal bone fixation

Imported from abroad

Dates and Status

Oct 10, 2019

Oct 10, 2024