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"Ofa" Restuphao limb equipment (unsterilized) - Taiwan Registration 25d84ea78f819dd90c3a554cf94a5666

Access comprehensive regulatory information for "Ofa" Restuphao limb equipment (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 25d84ea78f819dd90c3a554cf94a5666 and manufactured by OFA BAMBERG GMBH. The authorized representative in Taiwan is MEDIBIOT CO., LTD..

This page provides complete technical specifications, regulatory compliance details. 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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25d84ea78f819dd90c3a554cf94a5666
Registration Details
Taiwan FDA Registration: 25d84ea78f819dd90c3a554cf94a5666
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Device Details

"Ofa" Restuphao limb equipment (unsterilized)
TW: โ€œๆญๆณ•โ€่•พ่ฉฉๅพทๅฏถ่‚ข้ซ”่ฃๅ…ท (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

25d84ea78f819dd90c3a554cf94a5666

DHA04400711700

Company Information

Germany

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

Oct 14, 2008

Oct 14, 2018

Jun 22, 2022

Cancellation Information

Logged out

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