Taiwan FDA registration ce74529e2f3651dbf9c23c8e8f49cf5e

Corina implants

TW: 可麗媞植入劑

Taiwan·Risk Class 3·Keyan Biotechnology Co., Ltd. Biotechnology No. 1 Factory·Registered Mar 25, 2024 – Mar 25, 2029Active

Registration details

Analysis ID: ce74529e2f3651dbf9c23c8e8f49cf5e

Company information

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

Product details

Intended Use: Details are as detailed as approved Chinese instructions
Product Type (Level 1): I General, Plastic Surgery and Dermatology
Product Type (Level 2): I.9999 Miscellaneous
Import Information: Security Surveillance;; Domestic

Dates and status

Registration Date: Mar 25, 2024
Expiry Date: Mar 25, 2029

About this record

Access comprehensive regulatory information for Corina implants in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number ce74529e2f3651dbf9c23c8e8f49cf5e and manufactured by Keyan Biotechnology Co., Ltd. Biotechnology No. 1 Factory. The authorized representative in Taiwan is Keyan Biotechnology Co., Ltd. Biotechnology No. 1 Factory.

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.