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"Oslimme" electric plaster removal device (unsterilized) - Taiwan Registration f006bbe1d3824b262bdc96d252eba0f7

Access comprehensive regulatory information for "Oslimme" electric plaster removal 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 f006bbe1d3824b262bdc96d252eba0f7 and manufactured by OSCIMED SA. The authorized representative in Taiwan is YA HAI INTERNATIONAL INC..

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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f006bbe1d3824b262bdc96d252eba0f7
Registration Details
Taiwan FDA Registration: f006bbe1d3824b262bdc96d252eba0f7
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Device Details

"Oslimme" electric plaster removal device (unsterilized)
TW: โ€œๆญๆฐ็พŽโ€้›ปๅ‹•็Ÿณ่†ๅˆ‡้™คๅ™จๆขฐ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

f006bbe1d3824b262bdc96d252eba0f7

DHA04400744705

Company Information

Switzerland

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Equipment "Gypsum Removal Devices (N.5960)".

N Orthopedics

N.5960 ็Ÿณ่†ๆ‹†้™คๅ™จๆขฐ

import

Dates and Status

Feb 04, 2009

Feb 04, 2014

Mar 17, 2014

Cancellation Information

Logged out

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