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"Remel" Microorganism differentiation and identification device (Non-Sterile) - Taiwan Registration 9855418cbeb9b83eebc9546d27356934

Access comprehensive regulatory information for "Remel" Microorganism differentiation and identification device (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 9855418cbeb9b83eebc9546d27356934 and manufactured by REMEL EUROPE LIMITED. The authorized representative in Taiwan is CREATIVE LIFE SCIENCE CO., LTD..

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9855418cbeb9b83eebc9546d27356934
Registration Details
Taiwan FDA Registration: 9855418cbeb9b83eebc9546d27356934
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Device Details

"Remel" Microorganism differentiation and identification device (Non-Sterile)
TW: "้Šณ้‚" ๅพฎ็”Ÿ็‰ฉ้‘‘ๅˆฅๅŠๆธฌๅฎšๅ™จๆ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

9855418cbeb9b83eebc9546d27356934

Ministry of Health Medical Device Import No. 020515

DHA09402051505

Company Information

United Kingdom

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Microbial Identification and Measurement Equipment (C.2660)".

C Immunology and microbiology devices

C2660 Microbial identification and assay equipment

Imported from abroad

Dates and Status

Jun 03, 2019

Jun 03, 2024