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"Dybo" Diarrhoeagenic E coli PCR kit (Non-Sterile) - Taiwan Registration b76f7620c558ccc5b1d755bc3380ea0d

Access comprehensive regulatory information for "Dybo" Diarrhoeagenic E coli PCR kit (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 b76f7620c558ccc5b1d755bc3380ea0d and manufactured by SSI Diagnostica. The authorized representative in Taiwan is DYBO ENTERPRISE COMPANY LIMITED.

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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b76f7620c558ccc5b1d755bc3380ea0d
Registration Details
Taiwan FDA Registration: b76f7620c558ccc5b1d755bc3380ea0d
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Device Details

"Dybo" Diarrhoeagenic E coli PCR kit (Non-Sterile)
TW: "ๅธๅš"ๅคง่…ธๆกฟ่Œๅพฎ็”Ÿ็‰ฉ้‘‘ๅฎš่ฉฆๅŠ‘ๅฅ—็ต„(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

b76f7620c558ccc5b1d755bc3380ea0d

Ministry of Health Medical Device Import No. 019768

DHA09401976808

Company Information

Denmark

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "E. coli Serological Reagent (C.3255)".

C Immunology and microbiology devices

C3255 E. coli serum reagent

Imported from abroad

Dates and Status

Nov 02, 2018

Nov 02, 2023