"Perrigo" ScarAway Silicone scar management product (Non-Sterile) - Taiwan Registration 7d08193dfd73e5e16635bc0469031613
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 7d08193dfd73e5e16635bc0469031613 and manufactured by PERRIGO COMPANY PLC. The authorized representative in Taiwan is JEHOVAH-JIREH ENTERPRISE CO., LTD..
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.
Device Details
Registration Details
7d08193dfd73e5e16635bc0469031613
Ministry of Health Medical Device Import No. 020619
DHA09402061904
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
Jul 04, 2019
Jul 04, 2024