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"Hekoma" upper limb rehabilitation device (unsterilized)  - Taiwan Registration 1b729d68c71c7b00b84cc9eec413d42e

Access comprehensive regulatory information for "Hekoma" upper limb rehabilitation device (unsterilized)  in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 1b729d68c71c7b00b84cc9eec413d42e and manufactured by HOCOMA AT. The authorized representative in Taiwan is AMPLE MEDICAL INSTRUMENTS CO., LTD..

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1b729d68c71c7b00b84cc9eec413d42e
Registration Details
Taiwan FDA Registration: 1b729d68c71c7b00b84cc9eec413d42e
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Device Details

"Hekoma" upper limb rehabilitation device (unsterilized) 
TW: “賀可瑪”上肢復健裝置(未滅菌) 
Risk Class 1
Cancelled

Registration Details

1b729d68c71c7b00b84cc9eec413d42e

DHA04400674304

Company Information

Switzerland

Product Details

Limited to the first level recognition range of limb equipment (O.3475) of the Measures for the Administration of Medical Devices.

o Physical Medical Sciences

O.3475 Limb fittings

import

Dates and Status

May 12, 2008

May 12, 2013

Mar 14, 2012

Cancellation Information

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