Taiwan FDA registration 980337d252e4fc98c4a3182826fd33ca

"Triple" Continuous Passive Motion Device (Non-Sterile)

TW: "崔普" 連續式被動關節活動器(未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·KINETEC SAS·Registered Feb 09, 2018 – Feb 09, 2023Expired
Registration details
Analysis ID
980337d252e4fc98c4a3182826fd33ca
License Form
Ministry of Health Medical Device Import No. 018809
Customs Code
DHA09401880904
Company information
Manufacturer
KINETEC SAS
Manufacturer Country
France
Product details
Intended Use
Limited to the first level identification range of the Measures for the Administration of Medical Devices "Continuous Passive Joint Activator (O.0006)".
Product Type (Level 1)
o Equipment for physical medicine
Product Type (Level 2)
O0006 Continuous Passive Joint Activator
Import Information
Imported from abroad
Dates and status
Registration Date
Feb 09, 2018
Expiry Date
Feb 09, 2023
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About this record

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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