Taiwan FDA registration 9f34d275f832558533f4208ba85f004f

HYADERMIS LA Facial Dermal Implant

TW: 海德密絲輕感皮下填補劑

Taiwan·Risk Class 3·MD·Keyan Biotechnology Co., Ltd. Biotechnology No. 1 Factory·Registered Nov 16, 2013 – Nov 16, 2028Active

Registration details

Analysis ID: 9f34d275f832558533f4208ba85f004f
License Form: Ministry of Health Medical Device Manufacturing No. 004234

Company information

Manufacturer: Keyan Biotechnology Co., Ltd. Biotechnology No. 1 Factory
Manufacturer Country: Taiwan, Province of China
Authorized Representative: SCIVISION BIOTECH INC.

Product details

Intended Use: For details, it is Chinese approved copy of the imitation order
Product Type (Level 1): I General and plastic surgical devices
Product Type (Level 2): I0007 Hyaluronic acid implants
Import Information: Produced in Taiwan, China

Dates and status

Registration Date: Nov 16, 2013
Expiry Date: Nov 16, 2028

About this record

Access comprehensive regulatory information for HYADERMIS LA Facial Dermal Implant in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 9f34d275f832558533f4208ba85f004f and manufactured by Keyan Biotechnology Co., Ltd. Biotechnology No. 1 Factory. The authorized representative in Taiwan is SCIVISION BIOTECH INC..

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