Taiwan FDA registration 5ff594ac635d7e7ddc76c91a968861ef

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

TW: "阿莫特" 連續式被動關節活動器 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·ORMED GMBH·Registered Jul 03, 2018 – Jul 03, 2028Active
Registration details
Analysis ID
5ff594ac635d7e7ddc76c91a968861ef
License Form
Ministry of Health Medical Device Import No. 019256
Customs Code
DHA09401925607
Company information
Manufacturer
ORMED GMBH
Manufacturer Country
Germany
Authorized Representative
LUSH INDUSTRIAL CO., LTD.
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
Jul 03, 2018
Expiry Date
Jul 03, 2028
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About this record

Access comprehensive regulatory information for "ARTROMOT" 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 5ff594ac635d7e7ddc76c91a968861ef and manufactured by ORMED GMBH. The authorized representative in Taiwan is LUSH INDUSTRIAL CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including MEDIREHA 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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