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Bidi airfoil safety blood collection kit - Taiwan Registration 39260424b73fc636fbcf03fdc11d9243

Access comprehensive regulatory information for Bidi airfoil safety blood collection kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 39260424b73fc636fbcf03fdc11d9243 and manufactured by NIPRO MEDICAL INDUSTRIES LTD., TATEBAYASHI PLANT. 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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39260424b73fc636fbcf03fdc11d9243
Registration Details
Taiwan FDA Registration: 39260424b73fc636fbcf03fdc11d9243
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Device Details

Bidi airfoil safety blood collection kit
TW: ๅฟ…ๅธ็ฟผๅž‹ๅฎ‰ๅ…จๆŽก่ก€ๅฅ—็ต„
Risk Class 2

Registration Details

39260424b73fc636fbcf03fdc11d9243

DHA00602273108

Product Details

For details, it is Chinese approved copy of the imitation order

A Clinical chemistry and clinical toxicology

A.1675 Blood collection equipment

Contract manufacturing;; input

Dates and Status

Oct 24, 2011

Oct 24, 2026