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“BD” Q-Syte Luer Access Site Extension Sets - Taiwan Registration 1d5ee99707a38aaef6f741cd91fbd9a1

Access comprehensive regulatory information for “BD” Q-Syte Luer Access Site Extension Sets in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1d5ee99707a38aaef6f741cd91fbd9a1 and manufactured by BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.. 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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1d5ee99707a38aaef6f741cd91fbd9a1
Registration Details
Taiwan FDA Registration: 1d5ee99707a38aaef6f741cd91fbd9a1
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Device Details

“BD” Q-Syte Luer Access Site Extension Sets
TW: “必帝”延長型無針式輸液套接頭。“BD”延長型無針式輸液套接頭。
Risk Class 2
MD

Registration Details

1d5ee99707a38aaef6f741cd91fbd9a1

Department of Health Medical Device Import No. 019235

DHA00601923502

Product Details

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

J General hospital and personal use equipment

J5440 Intravascular infusion sleeve

Imported from abroad

Dates and Status

Sep 25, 2008

Sep 25, 2028