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“DAKO” PD-L1 IHC 28-8 pharmDx - Taiwan Registration 3dee28b3ef67d15337eac0cbfc3961d0

Access comprehensive regulatory information for “DAKO” PD-L1 IHC 28-8 pharmDx in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 3dee28b3ef67d15337eac0cbfc3961d0 and manufactured by Agilent Technologies, Inc.. The authorized representative in Taiwan is SCN TRADING COMPANY LIMITED.

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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3dee28b3ef67d15337eac0cbfc3961d0
Registration Details
Taiwan FDA Registration: 3dee28b3ef67d15337eac0cbfc3961d0
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Device Details

“DAKO” PD-L1 IHC 28-8 pharmDx
TW: “達克” PD-L1免疫組織化學染色28-8檢測套組
Risk Class 3
MD

Registration Details

3dee28b3ef67d15337eac0cbfc3961d0

Ministry of Health Medical Device Import No. 029492

DHA05602949205

Company Information

United States

Product Details

New performance: detailed as approved Chinese instructions. Performance: Details as detailed in the approved Chinese specification.

B Hematology and pathology devices

B1860 Immunopathological histochemical reagents and kits

Imported from abroad

Dates and Status

Feb 16, 2017

Feb 16, 2027