Taiwan FDA registration be5c10acc301dbc3e1c76aa2e2eeceaf

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

TW: "迪雅仕" 微生物樣本收集及輸送器材 (未滅菌)

Taiwan·Risk Class 1·MD·DIESSE DIAGNOSTICA SENESE S.P.A.·Registered May 17, 2019 – May 17, 2024Expired

Registration details

Analysis ID: be5c10acc301dbc3e1c76aa2e2eeceaf
License Form: Ministry of Health Medical Device Import No. 020459
Customs Code: DHA09402045908

Company information

Manufacturer: DIESSE DIAGNOSTICA SENESE S.P.A.
Manufacturer Country: Italy
Authorized Representative: GRAND MARQUIS CO., LTD.

Product details

Intended Use: Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Microbial Sample Collection and Delivery Equipment (C.2900)".
Product Type (Level 1): C Immunology and microbiology devices
Product Type (Level 2): C2900 Microbial sample collection and delivery device
Import Information: Imported from abroad

Dates and status

Registration Date: May 17, 2019
Expiry Date: May 17, 2024

About this record

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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