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"Parkell" Retraction Paste (Non-Sterile) - Taiwan Registration 22203872f5887643bebe237de25bff0a

Access comprehensive regulatory information for "Parkell" Retraction Paste (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 22203872f5887643bebe237de25bff0a and manufactured by PARKELL, INC.. The authorized representative in Taiwan is FRANKFURT TECHNOLOGY 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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22203872f5887643bebe237de25bff0a
Registration Details
Taiwan FDA Registration: 22203872f5887643bebe237de25bff0a
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Device Details

"Parkell" Retraction Paste (Non-Sterile)
TW: "ๆดพๅ…‹" ๆŽ’้ฝฆ่† (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

22203872f5887643bebe237de25bff0a

Ministry of Health Medical Device Import No. 019467

DHA09401946707

Company Information

United States

Product Details

Limited to the first level identification range of the gingival line (F.0001) of the medical equipment management method.

F Dental devices

F0001 Gingival drain line

Imported from abroad

Dates and Status

Aug 08, 2018

Aug 08, 2028