Taiwan FDA registration de1ca5cbd4049513f5b6d9d3730be6b3

"Beckman Coulter" automatic high-speed specimen conveyor (unsterilized)

TW: “貝克曼庫爾特”全自動高速檢體輸送裝置 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·BECKMAN COULTER BIOMEDICAL GMBH·Registered Aug 02, 2021 – Aug 02, 2026Cancelled
Registration details
Analysis ID
de1ca5cbd4049513f5b6d9d3730be6b3
Customs Code
DHA09402259500
Company information
Manufacturer Country
Germany
Product details
Intended Use
Limited to the first level identification range of the "Individual Photometric Chemistry Analyzer for Clinical Use (A.2160)" of the Measures for the Classification and Grading of Medical Devices.
Product Type (Level 1)
A Clinical chemistry and clinical toxicology
Product Type (Level 2)
A.2160 Individual Photometric Chemistry Analyzer for Clinical Use
Import Information
Input;; QMS/QSD
Dates and status
Registration Date
Aug 02, 2021
Expiry Date
Aug 02, 2026
Cancellation Date
Sep 30, 2021
Cancellation information
Status
Logged out
Reason
轉為登錄字號
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About this record

Access comprehensive regulatory information for "Beckman Coulter" automatic high-speed specimen conveyor (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number de1ca5cbd4049513f5b6d9d3730be6b3 and manufactured by BECKMAN COULTER BIOMEDICAL GMBH. The authorized representative in Taiwan is BECKMAN COULTER TAIWAN INC., TAIWAN BRANCH (U.S.A.).

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Beckman Coulter Biomedical GmbH, and 1 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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