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“UNIMAX” Quick-Guard Wound retractor(sterile) - Taiwan Registration 40c172332348b1dad60d1b37cb72c102

Access comprehensive regulatory information for “UNIMAX” Quick-Guard Wound retractor(sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 40c172332348b1dad60d1b37cb72c102 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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40c172332348b1dad60d1b37cb72c102
Registration Details
Taiwan FDA Registration: 40c172332348b1dad60d1b37cb72c102
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Device Details

“UNIMAX” Quick-Guard Wound retractor(sterile)
TW: “普威”傷口保護套(滅菌)
Risk Class 2
MD

Registration Details

40c172332348b1dad60d1b37cb72c102

Ministry of Health Medical Device Manufacturing No. 005886

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

Jul 21, 2017

Jul 21, 2027