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“SUNDER” Endo Bag - Taiwan Registration 06d3a46060a6ced1ecf58e03d2719de6

Access comprehensive regulatory information for “SUNDER” Endo Bag in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 06d3a46060a6ced1ecf58e03d2719de6 and manufactured by Shande Biochemical Technology Co., Ltd. is loyal to the factory. The authorized representative in Taiwan is SUNDER BIOMEDICAL TECH. 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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06d3a46060a6ced1ecf58e03d2719de6
Registration Details
Taiwan FDA Registration: 06d3a46060a6ced1ecf58e03d2719de6
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Device Details

“SUNDER” Endo Bag
TW: “善德”取物袋
Risk Class 2
MD

Registration Details

06d3a46060a6ced1ecf58e03d2719de6

Ministry of Health Medical Device Manufacturing No. 006905

Company Information

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

Jun 24, 2020

Jun 24, 2025