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Lumipulse G PIVKA-II Calibrators set - Taiwan Registration dd2c0a611dd6e7b75b72dae7562ea972

Access comprehensive regulatory information for Lumipulse G PIVKA-II Calibrators set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number dd2c0a611dd6e7b75b72dae7562ea972 and manufactured by FUJIREBIO INC., HACHIOJI FACILITY. The authorized representative in Taiwan is Grand Marquis IVD CO., LTD..

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dd2c0a611dd6e7b75b72dae7562ea972
Registration Details
Taiwan FDA Registration: dd2c0a611dd6e7b75b72dae7562ea972
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Device Details

Lumipulse G PIVKA-II Calibrators set
TW: ้Œ„็ง˜ๅธ•ๆ–ฏG็•ฐๅธธๅ‡่ก€้…ถๅŽŸๆจ™ๆบ–ๅ“็ต„
Risk Class 2
MD

Registration Details

dd2c0a611dd6e7b75b72dae7562ea972

Ministry of Health Medical Device Import No. 025898

DHA05602589800

Company Information

Product Details

This product is used for the correction of prothrombin detection reagents for Pas G abnormalities.

A Clinical chemistry and clinical toxicology

A1150 calibrate

Imported from abroad

Dates and Status

Feb 20, 2014

Feb 20, 2029