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"Picatech" Herpes Patch (Non-Sterile) - Taiwan Registration 9de9c5fb3bc4e50c023e9fcd90df0988

Access comprehensive regulatory information for "Picatech" Herpes Patch (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 9de9c5fb3bc4e50c023e9fcd90df0988 and manufactured by PIETRASANTA PHARMA S. P. A.. The authorized representative in Taiwan is PICATECH 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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9de9c5fb3bc4e50c023e9fcd90df0988
Registration Details
Taiwan FDA Registration: 9de9c5fb3bc4e50c023e9fcd90df0988
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Device Details

"Picatech" Herpes Patch (Non-Sterile)
TW: "ๅฑ็ฟ”" ็šฐ็–นๅ‚ทๅฃไฟ่ญท่ฒผ(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

9de9c5fb3bc4e50c023e9fcd90df0988

Ministry of Health Medical Device Import No. 021259

DHA09402125905

Company Information

Product Details

Limited to the first-level identification range of the Measures for the Administration of Medical Devices "Hydrophilic Wound Covering Materials (I.4018)".

I General and plastic surgical devices

I4018 Hydrophilic trauma coverings

Imported from abroad

Dates and Status

Feb 12, 2020

Feb 12, 2025