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"Sindeli" Clinical Sounder (Unsterilized) - Taiwan Registration ab49cd8a1cf3c59096329f6c396dfd31

Access comprehensive regulatory information for "Sindeli" Clinical Sounder (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ab49cd8a1cf3c59096329f6c396dfd31 and manufactured by Syntellix AG. The authorized representative in Taiwan is MEDLION BIOTECH 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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ab49cd8a1cf3c59096329f6c396dfd31
Registration Details
Taiwan FDA Registration: ab49cd8a1cf3c59096329f6c396dfd31
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Device Details

"Sindeli" Clinical Sounder (Unsterilized)
TW: "ไฟกๅพท็ซ‹" ่‡จๅบŠ็”จๆธฌๆทฑ่จˆ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

ab49cd8a1cf3c59096329f6c396dfd31

DHA09402169703

Company Information

Germany

Product Details

Limited to the first level identification range of the classification and grading management measures for medical equipment "Clinical Sothymetry (N.4300)".

N Orthopedics

N.4300 ่‡จๅบŠ็”จๆธฌๆทฑ่จˆ

Input;; QMS/QSD

Dates and Status

Jul 03, 2020

Jul 03, 2025

Nov 29, 2024