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RenehaVis - Taiwan Registration 8a41a07aea312ae5243e6addc4e0ae88

Access comprehensive regulatory information for RenehaVis in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 8a41a07aea312ae5243e6addc4e0ae88 and manufactured by MDT Intโ€™l S.A.. The authorized representative in Taiwan is HOLYLIFE BIOPHARMA CO., LTD..

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8a41a07aea312ae5243e6addc4e0ae88
Registration Details
Taiwan FDA Registration: 8a41a07aea312ae5243e6addc4e0ae88
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Device Details

RenehaVis
TW: ๅŠ›ๆฌฃ็ถญ้—œ็ฏ€ๅ…งๆณจๅฐ„ๅŠ‘
Risk Class 3
MD

Registration Details

8a41a07aea312ae5243e6addc4e0ae88

Ministry of Health Medical Device Import No. 031890

DHA05603189009

Company Information

Switzerland

Product Details

Provides lubrication for patients with degenerative knee arthritis to reduce the symptoms of joint pain.

N Orthopedic devices

N0003 Hyaluronic acid implants for the joint cavity

Imported from abroad

Dates and Status

May 21, 2019

May 21, 2024