Taiwan FDA registration af2166064c5a7053af46f2f0667c98af

Feiyide gel (unsterilized)

TW: 飛宜得凝膠 (未滅菌)

Taiwan·Risk Class 1·A. MENARINI ASIA- PACIFIC HOLDINGS PTE. LTD..;; PT MENARINI INDRIA LABORATORIES·Registered Nov 21, 2014 – Nov 21, 2029Active

Registration details

Analysis ID: af2166064c5a7053af46f2f0667c98af
Customs Code: DHA09401468801

Company information

Manufacturer: A. MENARINI ASIA- PACIFIC HOLDINGS PTE. LTD..;; PT MENARINI INDRIA LABORATORIES
Manufacturer Country: Indonesia;;Singapore
Authorized Representative: A. MENARINI SINGAPORE PTE. LTD. TAIWAN BRANCH

Product details

Intended Use: Limited to the first level identification scope of the Measures for the Classification and Grading of Medical Devices "Scar Treatment Silicone Products (I.4025)".
Product Type (Level 1): I General, Plastic Surgery and Dermatology
Product Type (Level 2): I.4025 Silicone products for scar treatment
Import Information: Input;; Contract manufacturing

Dates and status

Registration Date: Nov 21, 2014
Expiry Date: Nov 21, 2029

About this record

Access comprehensive regulatory information for Feiyide gel (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number af2166064c5a7053af46f2f0667c98af and manufactured by A. MENARINI ASIA- PACIFIC HOLDINGS PTE. LTD..;; PT MENARINI INDRIA LABORATORIES. The authorized representative in Taiwan is A. MENARINI SINGAPORE PTE. LTD. TAIWAN BRANCH.

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.