Taiwan FDA registration 2b0a91d9ddf69b7baec0cc6e73b0574e

VEJOKNEE Synovial Fluid Supplement

TW: 飛捷益關節腔注射劑

Taiwan·Risk Class 3·MD·Keyan Biotechnology Co., Ltd. Biotechnology No. 1 Factory·Registered May 17, 2022 – May 17, 2027Active

Registration details

Analysis ID: 2b0a91d9ddf69b7baec0cc6e73b0574e
License Form: Ministry of Health Medical Device Manufacturing No. 007392

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): N Orthopedics
Product Type (Level 2): N0003 Hyaluronic acid implants for the joint cavity
Import Information: Produced in Taiwan, China; Security monitoring

Dates and status

Registration Date: May 17, 2022
Expiry Date: May 17, 2027

About this record

Access comprehensive regulatory information for VEJOKNEE Synovial Fluid Supplement in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 2b0a91d9ddf69b7baec0cc6e73b0574e 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.