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"Perrigo" ScarAway Silicone scar management product (Non-Sterile) - Taiwan Registration 1c23880e68bf183d1f4dc72f8763c959

Access comprehensive regulatory information for "Perrigo" ScarAway Silicone scar management product (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 1c23880e68bf183d1f4dc72f8763c959 and manufactured by PERRIGO COMPANY PLC. The authorized representative in Taiwan is WEIYOU TECH INC..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including PERRIGO COMPANY PLC, and 1 recent registrations in the same category. 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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1c23880e68bf183d1f4dc72f8763c959
Registration Details
Taiwan FDA Registration: 1c23880e68bf183d1f4dc72f8763c959
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Device Details

"Perrigo" ScarAway Silicone scar management product (Non-Sterile)
TW: "ๅŸน็‘žๅ…‹" ็–ค็—•่™•็†็Ÿฝ่† ็”ขๅ“(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

1c23880e68bf183d1f4dc72f8763c959

Ministry of Health Medical Device Import No. 019516

DHA09401951607

Company Information

United States

Product Details

Limited to the first-level recognition range of the Measures for the Administration of Medical Devices "Scar Treatment Silicone Products (I.4025)".

I General and plastic surgical devices

I4025 Scar Treatment Silicone Products

Imported from abroad

Dates and Status

Aug 21, 2018

Aug 21, 2023

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