Taiwan FDA registration 1c23880e68bf183d1f4dc72f8763c959

"Perrigo" ScarAway Silicone scar management product (Non-Sterile)

TW: "培瑞克" 疤痕處理矽膠產品(未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·PERRIGO COMPANY PLC·Registered Aug 21, 2018 – Aug 21, 2023Expired
Registration details
Analysis ID
1c23880e68bf183d1f4dc72f8763c959
License Form
Ministry of Health Medical Device Import No. 019516
Customs Code
DHA09401951607
Company information
Manufacturer Country
United States
Authorized Representative
WEIYOU TECH INC.
Product details
Intended Use
Limited to the first-level recognition range of the Measures for the Administration of Medical Devices "Scar Treatment Silicone Products (I.4025)".
Product Type (Level 1)
I General and plastic surgical devices
Product Type (Level 2)
I4025 Scar Treatment Silicone Products
Import Information
Imported from abroad
Dates and status
Registration Date
Aug 21, 2018
Expiry Date
Aug 21, 2023
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About this record

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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