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"Pittiai" blood bank centrifuge for in vitro diagnostics (unsterilized) - Taiwan Registration dbfcc923d849f279d668873fb43c2731

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 dbfcc923d849f279d668873fb43c2731 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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dbfcc923d849f279d668873fb43c2731
Registration Details
Taiwan FDA Registration: dbfcc923d849f279d668873fb43c2731
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Device Details

"Pittiai" blood bank centrifuge for in vitro diagnostics (unsterilized)
TW: "็•ขๅ คๆ„›" ้ซ”ๅค–่จบๆ–ท็”จ่ก€ๅบซ้›ขๅฟƒๆฉŸ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

dbfcc923d849f279d668873fb43c2731

DHA08401529300

Company Information

Product Details

Limited to the classification and grading management method of medical equipment, in vitro diagnostic blood bank centrifuge (B.9275) first level identification range.

B Hematology, pathology, and genetics

B.9275 Blood bank centrifuge for in vitro diagnostics

Input;; QMS/QSD

Dates and Status

Oct 01, 2021

Oct 31, 2025

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