Taiwan FDA registration 2b7e7dac97839e89caccb20e165881ed

"HOKOMA" Lokma isokinetic muscle strength test evaluation system (unsterilized)

TW: "賀可瑪" 洛克美等速肌力試驗評估系統 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·HOCOMA AT·Registered Oct 01, 2021 – Oct 31, 2027Active
Registration details
Analysis ID
2b7e7dac97839e89caccb20e165881ed
Customs Code
DHA08401125406
Company information
Manufacturer
HOCOMA AT
Manufacturer Country
Switzerland
Authorized Representative
AMPLE MEDICAL INSTRUMENTS CO., LTD.
Product details
Intended Use
Limited to the classification and grading management method of medical equipment "isokinetic muscle strength test evaluation system (O.1925)" the first level recognition range.
Product Type (Level 1)
o Physical Medical Sciences
Product Type (Level 2)
O.1925 等速肌力試驗評估系統
Import Information
Input;; QMS/QSD
Dates and status
Registration Date
Oct 01, 2021
Expiry Date
Oct 31, 2027
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About this record

Access comprehensive regulatory information for "HOKOMA" Lokma isokinetic muscle strength test evaluation system (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 2b7e7dac97839e89caccb20e165881ed and manufactured by HOCOMA AT. The authorized representative in Taiwan is AMPLE MEDICAL INSTRUMENTS CO., LTD..

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