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“CareFusion” Manual Surgical Instrument for General Use (Non-Sterile) - Taiwan Registration 2871894fbdb6ce3daa494149dfd1b30b

Access comprehensive regulatory information for “CareFusion” Manual Surgical Instrument for General Use (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 2871894fbdb6ce3daa494149dfd1b30b and manufactured by CAREFUSION 209, INC.. The authorized representative in Taiwan is SYNGROWTH 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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2871894fbdb6ce3daa494149dfd1b30b
Registration Details
Taiwan FDA Registration: 2871894fbdb6ce3daa494149dfd1b30b
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Device Details

“CareFusion” Manual Surgical Instrument for General Use (Non-Sterile)
TW: "凱飛峻" 一般手術用手動式器械 (未滅菌)
Risk Class 1
MD
Cancelled

Registration Details

2871894fbdb6ce3daa494149dfd1b30b

Ministry of Health Medical Device Import No. 013913

DHA09401391300

Company Information

Slovakia

Product Details

I General and plastic surgical devices

I4800 General Surgery Manual Instrument

Imported from abroad

Dates and Status

Mar 05, 2014

Mar 05, 2019

Jun 22, 2022

Cancellation Information

Logged out

許可證已逾有效期