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"DIESSE" Microbiological Specimen Collection and Transport Device (Non-Sterile) - Taiwan Registration be5c10acc301dbc3e1c76aa2e2eeceaf

Access comprehensive regulatory information for "DIESSE" Microbiological Specimen Collection and Transport 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 be5c10acc301dbc3e1c76aa2e2eeceaf and manufactured by DIESSE DIAGNOSTICA SENESE S.P.A.. The authorized representative in Taiwan is GRAND MARQUIS CO., LTD..

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be5c10acc301dbc3e1c76aa2e2eeceaf
Registration Details
Taiwan FDA Registration: be5c10acc301dbc3e1c76aa2e2eeceaf
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Device Details

"DIESSE" Microbiological Specimen Collection and Transport Device (Non-Sterile)
TW: "่ฟช้›…ไป•" ๅพฎ็”Ÿ็‰ฉๆจฃๆœฌๆ”ถ้›†ๅŠ่ผธ้€ๅ™จๆ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

be5c10acc301dbc3e1c76aa2e2eeceaf

Ministry of Health Medical Device Import No. 020459

DHA09402045908

Company Information

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Microbial Sample Collection and Delivery Equipment (C.2900)".

C Immunology and microbiology devices

C2900 Microbial sample collection and delivery device

Imported from abroad

Dates and Status

May 17, 2019

May 17, 2024