Taiwan FDA registration 1770a6c3e522de0b41a960dc559fd5c5

"DIASORIN INC" Microorganism differentiation and identification device (Non-Sterile)

TW: "禮亞尚"微生物鑑別及測定器材 (未滅菌)

Taiwan·Risk Class 1·MD·DIASORIN INC.·Registered Sep 10, 2020 – Sep 10, 2025Expired

Registration details

Analysis ID: 1770a6c3e522de0b41a960dc559fd5c5
License Form: Ministry of Health Medical Device Import No. 021958
Customs Code: DHA09402195805

Company information

Manufacturer: DIASORIN INC.
Manufacturer Country: United States
Authorized Representative: EVERLIGHT BIOTECH(TAIWAN) CO., LTD.

Product details

Intended Use: Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Microbial Identification and Measurement Equipment (C.2660)".
Product Type (Level 1): C Immunology and microbiology devices
Product Type (Level 2): C2660 Microbial identification and assay equipment
Import Information: Imported from abroad

Dates and status

Registration Date: Sep 10, 2020
Expiry Date: Sep 10, 2025

About this record

Access comprehensive regulatory information for "DIASORIN INC" 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 1770a6c3e522de0b41a960dc559fd5c5 and manufactured by DIASORIN INC.. The authorized representative in Taiwan is EVERLIGHT BIOTECH(TAIWAN) CO., LTD..

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