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“CHI SHENG” REFRESH CLEAN SOLUTION - Taiwan Registration b0c76653f1e310755d9ff2a7c4cbc3d2

Access comprehensive regulatory information for “CHI SHENG” REFRESH CLEAN SOLUTION in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b0c76653f1e310755d9ff2a7c4cbc3d2 and manufactured by CHI SHENG PHARMA & BIOTECH CO., LTD. The authorized representative in Taiwan is CHI SHENG PHARMA & BIOTECH 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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b0c76653f1e310755d9ff2a7c4cbc3d2
Registration Details
Taiwan FDA Registration: b0c76653f1e310755d9ff2a7c4cbc3d2
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Device Details

“CHI SHENG” REFRESH CLEAN SOLUTION
TW: “濟生”芮視清沖洗液
Risk Class 2
MD

Registration Details

b0c76653f1e310755d9ff2a7c4cbc3d2

Ministry of Health Medical Device Manufacturing No. 005275

Company Information

Taiwan, Province of China

Product Details

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

J General hospital and personal use equipment

Produced in Taiwan, China

Dates and Status

Mar 15, 2016

Mar 15, 2026