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"Bidi" syringe - Taiwan Registration b372b18938c1fc8f0f66361821fb0573

Access comprehensive regulatory information for "Bidi" syringe in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b372b18938c1fc8f0f66361821fb0573 and manufactured by BECTON DICKINSON, S.A.. The authorized representative in Taiwan is BECTON DICKINSON HOLDINGS PTE. LTD. TAIWAN BRANCH (SINGAPORE).

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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b372b18938c1fc8f0f66361821fb0573
Registration Details
Taiwan FDA Registration: b372b18938c1fc8f0f66361821fb0573
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Device Details

"Bidi" syringe
TW: "ๅฟ…ๅธ"ๆณจๅฐ„็ญ’
Risk Class 2

Registration Details

b372b18938c1fc8f0f66361821fb0573

DHA00601121301

Company Information

Product Details

J General hospital and personal use equipment

J.5860 ๆดปๅกžๅผๆณจๅฐ„็ญ’

import

Dates and Status

Apr 27, 2005

Apr 27, 2030