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VEJOKNEE Synovial Fluid Supplement - Taiwan Registration 2b0a91d9ddf69b7baec0cc6e73b0574e

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.

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2b0a91d9ddf69b7baec0cc6e73b0574e
Registration Details
Taiwan FDA Registration: 2b0a91d9ddf69b7baec0cc6e73b0574e
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Device Details

VEJOKNEE Synovial Fluid Supplement
TW: ้ฃ›ๆท็›Š้—œ็ฏ€่…”ๆณจๅฐ„ๅŠ‘
Risk Class 3
MD

Registration Details

2b0a91d9ddf69b7baec0cc6e73b0574e

Ministry of Health Medical Device Manufacturing No. 007392

Company Information

Product Details

Details are as detailed as approved Chinese instructions

N Orthopedics

N0003 Hyaluronic acid implants for the joint cavity

Produced in Taiwan, China; Security monitoring

Dates and Status

May 17, 2022

May 17, 2027