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"Bidi" blood return vacuum blood collection needle - Taiwan Registration 6436b0baccb95bb66039306d680a6237

Access comprehensive regulatory information for "Bidi" blood return vacuum blood collection needle in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6436b0baccb95bb66039306d680a6237 and manufactured by BECTON DICKINSON MEDICAL(S) PTE. LTD.. 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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6436b0baccb95bb66039306d680a6237
Registration Details
Taiwan FDA Registration: 6436b0baccb95bb66039306d680a6237
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Device Details

"Bidi" blood return vacuum blood collection needle
TW: "ๅฟ…ๅธ" ๅ›ž่ก€ๅผ็œŸ็ฉบๆŽก่ก€้‡
Risk Class 2

Registration Details

6436b0baccb95bb66039306d680a6237

DHA00601089101

Product Details

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

J General hospital and personal use equipment

import

Dates and Status

Oct 26, 2004

Oct 26, 2029