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"CareFusion" Surgical Clipper(Non-sterile) - Taiwan Registration e61eaff3143c00932b99089b5e7d8ffa

Access comprehensive regulatory information for "CareFusion" Surgical Clipper(Non-sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e61eaff3143c00932b99089b5e7d8ffa and manufactured by CAREFUSION CORPORATION. The authorized representative in Taiwan is MEDITECHS INSTRUMENTS 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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e61eaff3143c00932b99089b5e7d8ffa
Registration Details
Taiwan FDA Registration: e61eaff3143c00932b99089b5e7d8ffa
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Device Details

"CareFusion" Surgical Clipper(Non-sterile)
TW: "ๅก็ฆ"ๅค–็ง‘้™คๆฏ›ๅ™จ(ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

e61eaff3143c00932b99089b5e7d8ffa

Ministry of Health Medical Device Import No. 014266

DHA09401426601

Company Information

United States

Product Details

I General and plastic surgical devices

I4800 General Surgery Manual Instrument

Imported from abroad

Dates and Status

Jun 19, 2014

Jun 19, 2019

Aug 05, 2022

Cancellation Information

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