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"Triple" Continuous Passive Motion Device (Non-Sterile) - Taiwan Registration 980337d252e4fc98c4a3182826fd33ca

Access comprehensive regulatory information for "Triple" Continuous Passive Motion Device (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 980337d252e4fc98c4a3182826fd33ca and manufactured by KINETEC SAS. The authorized representative in Taiwan is TRIAD ORTHOPEDIC PRODUCTS INDUSTRY CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including ORMED GMBH, and 1 recent registrations in the same category. 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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980337d252e4fc98c4a3182826fd33ca
Registration Details
Taiwan FDA Registration: 980337d252e4fc98c4a3182826fd33ca
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Device Details

"Triple" Continuous Passive Motion Device (Non-Sterile)
TW: "ๅด”ๆ™ฎ" ้€ฃ็บŒๅผ่ขซๅ‹•้—œ็ฏ€ๆดปๅ‹•ๅ™จ(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

980337d252e4fc98c4a3182826fd33ca

Ministry of Health Medical Device Import No. 018809

DHA09401880904

Company Information

France

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Continuous Passive Joint Activator (O.0006)".

o Equipment for physical medicine

O0006 Continuous Passive Joint Activator

Imported from abroad

Dates and Status

Feb 09, 2018

Feb 09, 2023

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