Taiwan FDA registration a1a2dc6b17b35fe48dca562c92f4ddd4

"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·ORMED GMBH·Registered Dec 29, 2016 – Dec 29, 2021Expired
Registration details
Analysis ID
a1a2dc6b17b35fe48dca562c92f4ddd4
License Form
Ministry of Health Medical Device Import No. 017345
Customs Code
DHA09401734509
Company information
Manufacturer
ORMED GMBH
Manufacturer Country
Germany
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
Dec 29, 2016
Expiry Date
Dec 29, 2021
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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 a1a2dc6b17b35fe48dca562c92f4ddd4 and manufactured by ORMED GMBH. 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 KINETEC SAS, 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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