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"BECKMAN COULTER" DxH 500 Series Diluent (Non-Sterile) - Taiwan Registration 0888e74c0316cdace47a7f8362c442bd

Access comprehensive regulatory information for "BECKMAN COULTER" DxH 500 Series 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 0888e74c0316cdace47a7f8362c442bd 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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0888e74c0316cdace47a7f8362c442bd
Registration Details
Taiwan FDA Registration: 0888e74c0316cdace47a7f8362c442bd
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Device Details

"BECKMAN COULTER" DxH 500 Series Diluent (Non-Sterile)
TW: "่ฒๅ…‹ๆ›ผๅบซ็ˆพ็‰น" DxH500็ณปๅˆ—่ก€็ƒ็จ€้‡‹ๅŠ‘ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

0888e74c0316cdace47a7f8362c442bd

Ministry of Health Medical Device Import No. 017674

DHA09401767402

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

Mar 31, 2017

Mar 31, 2027