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"Sieber" Radiology Patient Positioning Stent Equipment (Unsterilized) - Taiwan Registration e69ac2f536d7e46f4d01f9fbf514dcd1

Access comprehensive regulatory information for "Sieber" Radiology Patient Positioning Stent 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 e69ac2f536d7e46f4d01f9fbf514dcd1 and manufactured by BLESSING CATHAY CORPORATION. The authorized representative in Taiwan is Cypper Enterprises 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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e69ac2f536d7e46f4d01f9fbf514dcd1
Registration Details
Taiwan FDA Registration: e69ac2f536d7e46f4d01f9fbf514dcd1
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Device Details

"Sieber" Radiology Patient Positioning Stent Equipment (Unsterilized)
TW: โ€œๅธŒๆŸโ€ๆ”พๅฐ„็ง‘็—…ๆ‚ฃๅฎšไฝ็”จๆ”ฏๆžถๅ™จๆ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

e69ac2f536d7e46f4d01f9fbf514dcd1

Company Information

Taiwan, Province of China

Product Details

Limited to the first-level identification range of the Measures for the Administration of Medical Equipment "Stent for Radiology Patients (P.1830)".

P Radiology Science

P.1830 ๆ”พๅฐ„็ง‘็—…ๆ‚ฃ็”จๆ”ฏๆžถ

Contract manufacturing;; Domestic

Dates and Status

Sep 28, 2012

Sep 28, 2017

Aug 16, 2017

Cancellation Information

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