Taiwan FDA registration 39260424b73fc636fbcf03fdc11d9243

Bidi airfoil safety blood collection kit

TW: 必帝翼型安全採血套組

Taiwan·Risk Class 2·NIPRO MEDICAL INDUSTRIES LTD., TATEBAYASHI PLANT·Registered Oct 24, 2011 – Oct 24, 2026Active

Registration details

Analysis ID: 39260424b73fc636fbcf03fdc11d9243
Customs Code: DHA00602273108

Company information

Manufacturer: NIPRO MEDICAL INDUSTRIES LTD., TATEBAYASHI PLANT
Manufacturer Country: Japan
Authorized Representative: BECTON DICKINSON HOLDINGS PTE. LTD. TAIWAN BRANCH (SINGAPORE)

Product details

Intended Use: For details, it is Chinese approved copy of the imitation order
Product Type (Level 1): A Clinical chemistry and clinical toxicology
Product Type (Level 2): A.1675 Blood collection equipment
Import Information: Contract manufacturing;; input

Dates and status

Registration Date: Oct 24, 2011
Expiry Date: Oct 24, 2026

About this record

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.