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"Seegene" Mycoplasma Pneumoniae Test (non-sterile) - Taiwan Registration 490f17e7e46aa60ddf395abe308c381e

Access comprehensive regulatory information for "Seegene" Mycoplasma Pneumoniae Test (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 490f17e7e46aa60ddf395abe308c381e and manufactured by SEEGENE INC.. The authorized representative in Taiwan is MEDICARE PRODUCTS INC..

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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490f17e7e46aa60ddf395abe308c381e
Registration Details
Taiwan FDA Registration: 490f17e7e46aa60ddf395abe308c381e
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Device Details

"Seegene" Mycoplasma Pneumoniae Test (non-sterile)
TW: "่ฆ–ๅŸบ" ่‚บ็‚Ž้ปดๆผฟ่Œๆชขๆธฌ่ฉฆๅŠ‘ (ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

490f17e7e46aa60ddf395abe308c381e

Ministry of Health Medical Device Import No. 016372

DHA09401637207

Company Information

Korea, Republic of

Product Details

C Immunology and microbiology devices

C3375 Mycoplasma serum reagent

Imported from abroad

Dates and Status

Apr 08, 2016

Apr 08, 2021

Feb 21, 2017

Cancellation Information

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