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"Kennett" powered therapy unit (unsterilized) - Taiwan Registration a31572b6e3c403c41d5ef256ff9267e5

Access comprehensive regulatory information for "Kennett" powered therapy unit (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a31572b6e3c403c41d5ef256ff9267e5 and manufactured by KINETEC S.A.. The authorized representative in Taiwan is Yajin International Limited.

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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a31572b6e3c403c41d5ef256ff9267e5
Registration Details
Taiwan FDA Registration: a31572b6e3c403c41d5ef256ff9267e5
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Device Details

"Kennett" powered therapy unit (unsterilized)
TW: โ€œ่‚ฏๅฐผ็‰นโ€ๅ‹•ๅŠ›ๅผๆฒป็™‚ๆชฏ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

a31572b6e3c403c41d5ef256ff9267e5

DHA04400751904

Company Information

France

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Equipment "Powered Treatment Units (O.3760)".

o Physical Medical Sciences

O.3760 Powered therapy cage

import

Dates and Status

Feb 26, 2009

Feb 26, 2014

Jan 09, 2017

Cancellation Information

Logged out

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