Taiwan FDA registration fd727c920c29de7587240c0e36edd11f

“Horien” Extracellular Membrane

TW: “海昌”膠原再生薄膜

Taiwan·Risk Class 2·MD·HORIEN BIOCHEMICAL TECHNOLOGY CO., LTD.·Registered Feb 16, 2017 – Feb 16, 2027Active

Registration details

Analysis ID: fd727c920c29de7587240c0e36edd11f
License Form: Ministry of Health Medical Device Manufacturing No. 005701

Company information

Manufacturer: HORIEN BIOCHEMICAL TECHNOLOGY CO., LTD.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: HORIEN BIOCHEMICAL TECHNOLOGY CO., LTD.

Product details

Intended Use: For details, it is Chinese approved copy of the imitation order
Product Type (Level 1): F Dental devices
Product Type (Level 2): F3930 Tricalcium phosphate for alveolar bone restoration
Import Information: Produced in Taiwan, China

Dates and status

Registration Date: Feb 16, 2017
Expiry Date: Feb 16, 2027

About this record

Access comprehensive regulatory information for “Horien” Extracellular Membrane in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fd727c920c29de7587240c0e36edd11f and manufactured by HORIEN BIOCHEMICAL TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is HORIEN BIOCHEMICAL TECHNOLOGY CO., LTD..

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