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"Dybo" Escherichia coli Antisera Reagent (Non-Sterile) - Taiwan Registration 19135103ba7cbcad8fd9519114b2b469

Access comprehensive regulatory information for "Dybo" Escherichia coli Antisera Reagent (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 19135103ba7cbcad8fd9519114b2b469 and manufactured by SSI Diagnostica. The authorized representative in Taiwan is DYBO ENTERPRISE COMPANY LIMITED.

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19135103ba7cbcad8fd9519114b2b469
Registration Details
Taiwan FDA Registration: 19135103ba7cbcad8fd9519114b2b469
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Device Details

"Dybo" Escherichia coli Antisera Reagent (Non-Sterile)
TW: "ๅธๅš" ๅคง่…ธๆกฟ่ŒๆŠ—่ก€ๆธ…่ฉฆๅŠ‘(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

19135103ba7cbcad8fd9519114b2b469

Ministry of Health Medical Device Import No. 020994

DHA09402099404

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

Oct 31, 2019

Oct 31, 2024