Taiwan FDA registration bf653b5ff5eff464d1520d76dcea8e9e

"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 Dec 30, 2011 – Dec 30, 2026Cancelled
Registration details
Analysis ID
bf653b5ff5eff464d1520d76dcea8e9e
Customs Code
DHA04401125409
Company information
Manufacturer
HOCOMA AT
Manufacturer Country
Switzerland
Authorized Representative
AMPLE MEDICAL INSTRUMENTS CO., LTD.
Product details
Intended Use
Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Isokinetic Muscle Strength Test Evaluation System (O.1925)".
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
QMS/QSD;; 輸入
Dates and status
Registration Date
Dec 30, 2011
Expiry Date
Dec 30, 2026
Cancellation Date
Sep 30, 2021
Cancellation information
Status
Logged out
Reason
轉為登錄字號
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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 bf653b5ff5eff464d1520d76dcea8e9e 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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