Taiwan FDA registration c929bd06893da02b9c25e6529d5ac7ac

"Pittiai" blood bank centrifuge for in vitro diagnostics (unsterilized)

TW: "畢堤愛" 體外診斷用血庫離心機 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·B.T.I. BIOTECHNOLOGY INSTITUTE S.L.·Registered Jun 03, 2015 – Jun 03, 2025Cancelled
Registration details
Analysis ID
c929bd06893da02b9c25e6529d5ac7ac
Customs Code
DHA09401529306
Company information
Manufacturer Country
Spain
Authorized Representative
SEQPRO, INC.
Product details
Intended Use
Limited to the first level identification range of blood bank centrifuge (B.9275) for in vitro diagnostic of medical equipment management methods.
Product Type (Level 1)
B Hematology, pathology, and genetics
Product Type (Level 2)
B.9275 Blood bank centrifuge for in vitro diagnostics
Import Information
Input;; QMS/QSD
Dates and status
Registration Date
Jun 03, 2015
Expiry Date
Jun 03, 2025
Cancellation Date
Sep 30, 2021
Cancellation information
Status
Logged out
Reason
轉為登錄字號
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About this record

Access comprehensive regulatory information for "Pittiai" blood bank centrifuge for in vitro diagnostics (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number c929bd06893da02b9c25e6529d5ac7ac and manufactured by B.T.I. BIOTECHNOLOGY INSTITUTE S.L.. The authorized representative in Taiwan is SEQPRO, INC..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including B.T.I. BIOTECHNOLOGY INSTITUTE S.L., and 1 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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