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"Difu Xindis" Provisional Sample Plate (Unextinguished) - Taiwan Registration 74596530fc9ff21fa3f728e90e70b81f

Access comprehensive regulatory information for "Difu Xindis" Provisional Sample Plate (Unextinguished) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 74596530fc9ff21fa3f728e90e70b81f and manufactured by MEDOS INTERNATIONAL SARL. 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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74596530fc9ff21fa3f728e90e70b81f
Registration Details
Taiwan FDA Registration: 74596530fc9ff21fa3f728e90e70b81f
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Device Details

"Difu Xindis" Provisional Sample Plate (Unextinguished)
TW: โ€œๅธๅฏŒไฟก่ฟชๆ€โ€ ่‡จๅบŠ็”จๆจฃๆฟ(ๆœชๆป…่Œ)
Risk Class 1

Registration Details

74596530fc9ff21fa3f728e90e70b81f

DHA09402323300

Company Information

Switzerland

Product Details

Limited to the classification and grading management measures of medical equipment "Clinical Use Model (N.4800) First Level Identification Range".

N Orthopedics

N.4800 Sample plate for clinical use

QMS/QSD;; ่ผธๅ…ฅ

Dates and Status

Sep 04, 2023

Sep 04, 2028