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Timela Ratti line - Taiwan Registration f964e9ea0ff7a22cf88f92bc0610b61d

Access comprehensive regulatory information for Timela Ratti line in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f964e9ea0ff7a22cf88f92bc0610b61d and manufactured by Fuzhan Mei Technology Co., Ltd. Dongshan Factory. The authorized representative in Taiwan is DIAMOND BIOTECHNOLOGY 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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f964e9ea0ff7a22cf88f92bc0610b61d
Registration Details
Taiwan FDA Registration: f964e9ea0ff7a22cf88f92bc0610b61d
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Device Details

Timela Ratti line
TW: ๆ็พŽๆ‹‰ๆ‹‰ๆ็ทš
Risk Class 2

Registration Details

f964e9ea0ff7a22cf88f92bc0610b61d

Company Information

Taiwan, Province of China

Product Details

Details are as detailed as approved Chinese instructions

I General, Plastic Surgery and Dermatology

I.4840 Absorbable polydioxanone surgical joint

Domestic;; Contract manufacturing;; Security surveillance

Dates and Status

Dec 01, 2022

Dec 01, 2027