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“KUBTEC” Digital Specimen Radiography System - Taiwan Registration 60307e0b94e8a75384034031cb3def25

Access comprehensive regulatory information for “KUBTEC” Digital Specimen Radiography System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 60307e0b94e8a75384034031cb3def25 and manufactured by KUB Technologies Inc.. The authorized representative in Taiwan is PROMEDICS TECHNOLOGY 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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60307e0b94e8a75384034031cb3def25
Registration Details
Taiwan FDA Registration: 60307e0b94e8a75384034031cb3def25
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Device Details

“KUBTEC” Digital Specimen Radiography System
TW: “柯博特” 組織樣本數位化影像系統
Risk Class 2
MD

Registration Details

60307e0b94e8a75384034031cb3def25

Ministry of Health Medical Device Import No. 034863

DHA05603486308

Company Information

United States

Product Details

Details are as detailed as approved Chinese instructions

P Devices for radiology

P1680 stationary X-ray system

Imported from abroad

Dates and Status

Sep 17, 2021

Sep 17, 2026