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"BioSpeedia" Streptococcus Pneumoniae Kit (Non-Sterile) - Taiwan Registration 2f6edf9392b5544a879a5c8fdb4c00df

Access comprehensive regulatory information for "BioSpeedia" Streptococcus Pneumoniae 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 2f6edf9392b5544a879a5c8fdb4c00df and manufactured by BioSpeedia, SAS. The authorized representative in Taiwan is YOULUM BIOTECHNOLOGY CO., LTD..

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2f6edf9392b5544a879a5c8fdb4c00df
Registration Details
Taiwan FDA Registration: 2f6edf9392b5544a879a5c8fdb4c00df
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Device Details

"BioSpeedia" Streptococcus Pneumoniae Kit (Non-Sterile)
TW: "ๆ‹œๆญ้€Ÿ" ่‚บ็‚Ž้ˆ็ƒ่Œๆชข้ฉ—่ฉฆๅŠ‘็ต„ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

2f6edf9392b5544a879a5c8fdb4c00df

Ministry of Health Medical Device Import No. 019279

DHA09401927906

Company Information

France

Product Details

Restriction of medical device management methods Streptococcus belongs to the first level identification range of serum reagent (C.3740).

C Immunology and microbiology devices

C3740 Streptococcus serology

Imported from abroad

Dates and Status

Jul 06, 2018

Jul 06, 2023