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"BECKMAN COULTER" DxH 500 Diluent (Non-Sterile) - Taiwan Registration 53050e34591c735e07ba9eb5d2c34c65

Access comprehensive regulatory information for "BECKMAN COULTER" DxH 500 Diluent (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 53050e34591c735e07ba9eb5d2c34c65 and manufactured by BECKMAN COULTER GmbH. The authorized representative in Taiwan is BECKMAN COULTER TAIWAN INC., TAIWAN BRANCH (U.S.A.).

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53050e34591c735e07ba9eb5d2c34c65
Registration Details
Taiwan FDA Registration: 53050e34591c735e07ba9eb5d2c34c65
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Device Details

"BECKMAN COULTER" DxH 500 Diluent (Non-Sterile)
TW: "่ฒๅ…‹ๆ›ผๅบซ็ˆพ็‰น" DxH500่ก€็ƒ็จ€้‡‹ๅŠ‘ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

53050e34591c735e07ba9eb5d2c34c65

Ministry of Health Medical Device Import No. 016508

DHA09401650806

Company Information

Product Details

Limited to the first level identification range of blood cell thinners (B.8200) of the management methods for medical devices.

B Hematology and pathology devices

B8200 Blood cell thinner

Imported from abroad

Dates and Status

May 09, 2016

May 09, 2021