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“UNIMAX” Anti-Fog Solution (Sterile) - Taiwan Registration 8588f8f53084a83341a87d47c33619bb

Access comprehensive regulatory information for “UNIMAX” Anti-Fog Solution (Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8588f8f53084a83341a87d47c33619bb 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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8588f8f53084a83341a87d47c33619bb
Registration Details
Taiwan FDA Registration: 8588f8f53084a83341a87d47c33619bb
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Device Details

“UNIMAX” Anti-Fog Solution (Sterile)
TW: “普威”腹腔鏡用防霧油(滅菌)
Risk Class 2
MD

Registration Details

8588f8f53084a83341a87d47c33619bb

Ministry of Health Medical Device Manufacturing No. 006651

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

Dec 08, 2019

Dec 08, 2024