Taiwan FDA registration dab908f1db7af0760345cbc7bc2e80af

"Agilent" Microplate Readers (Non-sterile)

TW: "安捷倫" 微量盤偵測儀 (未滅菌)

Taiwan·Risk Class 1·MD·Agilent Technologies, Inc.·Registered May 23, 2022 – Oct 31, 2023Expired

Registration details

Analysis ID: dab908f1db7af0760345cbc7bc2e80af
License Form: Ministry of Health Medical Device Import Registration No. a00068
Customs Code: DHA084a0006805

Company information

Manufacturer: Agilent Technologies, Inc.
Manufacturer Country: United States
Authorized Representative: AGILENT TECHNOLOGIES TAIWAN LTD.

Product details

Intended Use: Limited to the first level identification range of the Measures for the Classification and Grading of Medical Devices "Colorimeter, Photometer or Spectrophotometer for Clinical Use (A.2300)".
Product Type (Level 1): A Clinical chemistry and clinical toxicology
Product Type (Level 2): A2300 Colorimeter, photometer, or spectrophotometer for clinical use

Dates and status

Registration Date: May 23, 2022
Expiry Date: Oct 31, 2023

About this record

Access comprehensive regulatory information for "Agilent" Microplate Readers (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 dab908f1db7af0760345cbc7bc2e80af and manufactured by Agilent Technologies, Inc.. The authorized representative in Taiwan is AGILENT TECHNOLOGIES TAIWAN LTD..

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