Pure Global

"Keai Fusen" Miller Manual instruments for general surgery (unsterilized)  - Taiwan Registration 6d7b1538c6377e61bb33399a56a4c595

Access comprehensive regulatory information for "Keai Fusen" Miller Manual instruments for general surgery (unsterilized)  in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 6d7b1538c6377e61bb33399a56a4c595 and manufactured by CAREFUSION. The authorized representative in Taiwan is CHAMPION MEDICAL CORPORATION.

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.

Free Database
Powered by Pure Global AI
89,000+ Devices
6d7b1538c6377e61bb33399a56a4c595
Registration Details
Taiwan FDA Registration: 6d7b1538c6377e61bb33399a56a4c595
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Keai Fusen" Miller Manual instruments for general surgery (unsterilized) 
TW: “客愛福生” 米樂 一般手術用手動式器械 (未滅菌) 
Risk Class 1
Cancelled

Registration Details

6d7b1538c6377e61bb33399a56a4c595

DHA04401085300

Company Information

United States

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Instruments for General Surgery (I.4800)".

I General, Plastic Surgery and Dermatology

I.4800 Hand Instruments for General Surgery

import

Dates and Status

Sep 19, 2011

Sep 19, 2021

Oct 12, 2023

Cancellation Information

Logged out

未展延而逾期者