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"Beckman Coulter" Coulter Blood Cell Diluent (Unsterilized) - Taiwan Registration 83c488619f60debc6933910143a11f59

Access comprehensive regulatory information for "Beckman Coulter" Coulter Blood Cell Diluent (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 83c488619f60debc6933910143a11f59 and manufactured by BECKMAN COULTER LABORATORY SYSTEMS (SUZHOU) CO., LTD.;; BECKMAN COULTER INC.. The authorized representative in Taiwan is BECKMAN COULTER TAIWAN INC., TAIWAN BRANCH (U.S.A.).

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83c488619f60debc6933910143a11f59
Registration Details
Taiwan FDA Registration: 83c488619f60debc6933910143a11f59
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Device Details

"Beckman Coulter" Coulter Blood Cell Diluent (Unsterilized)
TW: "่ฒๅ…‹ๆ›ผๅบซ็ˆพ็‰น" ๅบซ็ˆพ็‰น่ก€็ƒ็จ€้‡‹ๅŠ‘ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

83c488619f60debc6933910143a11f59

DHA09600235500

Product Details

Limited to the first level identification range of "blood cell thinners (B.8200)" of the Measures for the Classification and Grading of Medical Devices.

B Hematology, pathology, and genetics

B.8200 Hemocytodilant

Input;; Chinese goods

Dates and Status

Mar 30, 2015

Mar 30, 2030