Taiwan FDA registration 77777825df56f15c135c1bab3f0cc8fa

"Termao" Zima automatic blood cell collection system loop tube group

TW: “泰爾茂”齊瑪全自動血球收集系統迴路管組
Taiwan flagTaiwan·Risk Class 2·TERUMO BCT, INC.;; TFB MANUFACTURING SRL·Registered Jan 14, 2009 – Jan 14, 2029Active
Registration details
Analysis ID
77777825df56f15c135c1bab3f0cc8fa
Customs Code
DHA00601956102
Company information
Manufacturer Country
Costa Rica;;United States
Authorized Representative
TERUMO TAIWAN MEDICAL CO., LTD.
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
B Hematology, pathology, and genetics
Product Type (Level 2)
B.9100 Containers for the collection and disposal of blood and blood components
Import Information
import
Dates and status
Registration Date
Jan 14, 2009
Expiry Date
Jan 14, 2029
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About this record

Access comprehensive regulatory information for "Termao" Zima automatic blood cell collection system loop tube group in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 77777825df56f15c135c1bab3f0cc8fa and manufactured by TERUMO BCT, INC.;; TFB MANUFACTURING SRL. The authorized representative in Taiwan is TERUMO TAIWAN MEDICAL CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including Terumo BCT, Inc., TERUMO BCT, INC.;; TFB MANUFACTURING SRL, and 2 recent registrations in the same category. 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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