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“DPB” Cannula - Taiwan Registration b26e65263d11151ad22ad0719a62056e

Access comprehensive regulatory information for “DPB” Cannula in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b26e65263d11151ad22ad0719a62056e and manufactured by Dashun Factory of Chengru Biotechnology Co., Ltd. The authorized representative in Taiwan is DERMATO PLASTICA BEAUTY 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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b26e65263d11151ad22ad0719a62056e
Registration Details
Taiwan FDA Registration: b26e65263d11151ad22ad0719a62056e
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Device Details

“DPB” Cannula
TW: “呈汝” 鈍針
Risk Class 2
MD

Registration Details

b26e65263d11151ad22ad0719a62056e

Ministry of Health Medical Device Manufacturing No. 007961

Company Information

Taiwan, Province of China

Product Details

Details are as detailed as approved Chinese instructions

J General hospital and personal use equipment

J5570 Subcutaneous single-lumen needle

Produced in Taiwan, China

Dates and Status

Aug 14, 2023

Aug 14, 2028