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"Kinetec" Continuous Passive Motion Device (Non-sterile) - Taiwan Registration dc322b2a5c2518814b411794a7c44539

Access comprehensive regulatory information for "Kinetec" 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 dc322b2a5c2518814b411794a7c44539 and manufactured by KINETEC SAS. The authorized representative in Taiwan is MAGISTRAL ENTERPRISE, INC..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including KINETEC, 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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dc322b2a5c2518814b411794a7c44539
Registration Details
Taiwan FDA Registration: dc322b2a5c2518814b411794a7c44539
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Device Details

"Kinetec" Continuous Passive Motion Device (Non-sterile)
TW: "ๅฏ่€ๅพ—" ้€ฃ็บŒๅผ่ขซๅ‹•้—œ็ฏ€ๆดปๅ‹•ๅ™จ (ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

dc322b2a5c2518814b411794a7c44539

Ministry of Health Medical Device Import No. 018898

DHA09401889803

Company Information

France

Product Details

o Equipment for physical medicine

O0006 Continuous Passive Joint Activator

Imported from abroad

Dates and Status

Mar 15, 2018

Mar 15, 2023

May 19, 2021

Cancellation Information

Logged out

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