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"Quidel" Sofia S.pneumoniae FIA (Non-Sterile) - Taiwan Registration 50d55b503260293c9dea422dd8437b15

Access comprehensive regulatory information for "Quidel" Sofia S.pneumoniae FIA (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 50d55b503260293c9dea422dd8437b15 and manufactured by QUIDEL CORPORATION. The authorized representative in Taiwan is GRAND MARQUIS CO., LTD..

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.

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50d55b503260293c9dea422dd8437b15
Registration Details
Taiwan FDA Registration: 50d55b503260293c9dea422dd8437b15
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Device Details

"Quidel" Sofia S.pneumoniae FIA (Non-Sterile)
TW: "ๆœƒๅพ—" ่ˆ’ๅฆƒ้›…่‚บ็‚Ž้ˆ็ƒ่Œๅฟซ้€Ÿ่žขๅ…‰้…ต็ด ๅ…็–ซๅˆ†ๆžๆชขๆธฌๅฅ—็ต„ (ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

50d55b503260293c9dea422dd8437b15

Ministry of Health Medical Device Import No. 017025

DHA09401702504

Company Information

United States

Product Details

C Immunology and microbiology devices

C3740 Streptococcus serology

Imported from abroad

Dates and Status

Sep 26, 2016

Sep 26, 2021

Aug 31, 2023

Cancellation Information

Logged out

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