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"Difuxindis" Clinical Sounder (Unsterilized) - Taiwan Registration cb21bd1a28cfbddc22eacd6559ffdb5b

Access comprehensive regulatory information for "Difuxindis" 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 cb21bd1a28cfbddc22eacd6559ffdb5b and manufactured by Tyber Medical LLC. The authorized representative in Taiwan is JOHNSON & JOHNSON MEDICAL TAIWAN 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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cb21bd1a28cfbddc22eacd6559ffdb5b
Registration Details
Taiwan FDA Registration: cb21bd1a28cfbddc22eacd6559ffdb5b
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Device Details

"Difuxindis" Clinical Sounder (Unsterilized)
TW: โ€œๅธๅฏŒไฟก่ฟชๆ€โ€ ่‡จๅบŠ็”จๆธฌๆทฑ่จˆ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

cb21bd1a28cfbddc22eacd6559ffdb5b

DHA09402313204

Company Information

United States

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

May 25, 2023

May 25, 2028