"Perrigo" ScarAway Silicone scar management product (Non-Sterile)
Taiwan·Risk Class 1·MD·PERRIGO COMPANY PLC·Registered Jul 04, 2019 – Jul 04, 2024Expired- Analysis ID
- 7d08193dfd73e5e16635bc0469031613
- License Form
- Ministry of Health Medical Device Import No. 020619
- Customs Code
- DHA09402061904
- Manufacturer
- PERRIGO COMPANY PLC
- Manufacturer Country
- United States
- Authorized Representative
- JEHOVAH-JIREH ENTERPRISE CO., LTD.
- 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
- Registration Date
- Jul 04, 2019
- Expiry Date
- Jul 04, 2024
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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.