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貝克曼庫爾特庫爾特 DxH 紅血球溶解劑(未滅菌) - Taiwan Registration 77ad9a8543ad3803f5661d8104437e8b

Access comprehensive regulatory information for 貝克曼庫爾特庫爾特 DxH 紅血球溶解劑(未滅菌) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 77ad9a8543ad3803f5661d8104437e8b and manufactured by Beckman Coulter, Inc.. The authorized representative in Taiwan is BECKMAN COULTER TAIWAN INC., TAIWAN BRANCH (U.S.A.).

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77ad9a8543ad3803f5661d8104437e8b
Registration Details
Taiwan FDA Registration: 77ad9a8543ad3803f5661d8104437e8b
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Device Details

貝克曼庫爾特庫爾特 DxH 紅血球溶解劑(未滅菌)
Risk Class 1

Registration Details

77ad9a8543ad3803f5661d8104437e8b

DHA09402369407

Company Information

United States

Product Details

It is limited to the first-level identification scope of the "Erythrolytic Agents (B.8540)" of the Administrative Measures for the Classification and Grading of Medical Devices.

B Hematology, pathology, and genetics

B.8540 紅血球溶解劑

Input;; QMS/QSD

Dates and Status

Nov 28, 2024

Nov 28, 2029