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“UNIMAX” Single Port Access System (Sterile) - Taiwan Registration 0f37583f3ffa2f96694ac05ad32dc5ed

Access comprehensive regulatory information for “UNIMAX” Single Port Access System (Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0f37583f3ffa2f96694ac05ad32dc5ed and manufactured by Puwei International Co., Ltd. Yilan Factory. The authorized representative in Taiwan is UNIMAX MEDICAL SYSTEMS INC..

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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0f37583f3ffa2f96694ac05ad32dc5ed
Registration Details
Taiwan FDA Registration: 0f37583f3ffa2f96694ac05ad32dc5ed
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Device Details

“UNIMAX” Single Port Access System (Sterile)
TW: “普威”單孔多器械手術通路系統(滅菌)
Risk Class 2
MD

Registration Details

0f37583f3ffa2f96694ac05ad32dc5ed

Ministry of Health Medical Device Manufacturing No. 005901

Company Information

Taiwan, Province of China

Product Details

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

H Gastroenterology-urology devices

H1500 endoscope and accessories

Produced in Taiwan, China

Dates and Status

Sep 05, 2017

Sep 05, 2027