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"Yisi Suzhou" single-use tube stapler - Taiwan Registration c5b05fae2d2b65b10b2944e7f07dc9ad

Access comprehensive regulatory information for "Yisi Suzhou" single-use tube stapler in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c5b05fae2d2b65b10b2944e7f07dc9ad and manufactured by Ezisurg (Suzhou) Medical Co., Ltd.. The authorized representative in Taiwan is DR SHAO MD REGULATORY CONSULTANTS 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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c5b05fae2d2b65b10b2944e7f07dc9ad
Registration Details
Taiwan FDA Registration: c5b05fae2d2b65b10b2944e7f07dc9ad
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Device Details

"Yisi Suzhou" single-use tube stapler
TW: โ€œ้€ธๆ€่˜‡ๅทžโ€ไธ€ๆฌกๆ€งไฝฟ็”จ็ฎกๅž‹ๅปๅˆๅ™จ
Risk Class 2

Registration Details

c5b05fae2d2b65b10b2944e7f07dc9ad

DHA09200111607

Company Information

Product Details

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

I General, Plastic Surgery and Dermatology

I.4750 Implantable Joints

Input;; Chinese goods

Dates and Status

Mar 01, 2020

Mar 01, 2025