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"Dulac" blood bank centrifuge for in vitro diagnostics (unsterilized) - Taiwan Registration 608df277f4b24941b5415502f51ade0b

Access comprehensive regulatory information for "Dulac" 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 608df277f4b24941b5415502f51ade0b and manufactured by PRINTER DIAGNOSTICS. The authorized representative in Taiwan is SYNERGY BIOMEDICAL LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including PRINTER DIAGNOSTICS, 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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608df277f4b24941b5415502f51ade0b
Registration Details
Taiwan FDA Registration: 608df277f4b24941b5415502f51ade0b
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Device Details

"Dulac" blood bank centrifuge for in vitro diagnostics (unsterilized)
TW: "ๆœๆ‹‰ๅ…‹" ้ซ”ๅค–่จบๆ–ท็”จ่ก€ๅบซ้›ขๅฟƒๆฉŸ(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

608df277f4b24941b5415502f51ade0b

DHA09401978508

Company Information

United States

Product Details

Limited to the first level identification range of blood bank centrifuge (B.9275) for in vitro diagnostic of medical equipment management methods.

B Hematology, pathology, and genetics

B.9275 Blood bank centrifuge for in vitro diagnostics

QMS/QSD;; ่ผธๅ…ฅ

Dates and Status

Nov 06, 2018

Nov 06, 2023

Sep 30, 2021

Cancellation Information

Logged out

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