Taiwan FDA registration 7a8277076875edc825e89b7a4efbadab

"DAKO" Monoclonal Mouse Anti-Human PD-L1 22C3 (Non-Sterile)

TW: "達克" PD-L1 22C3單株抗體 (未滅菌)

Taiwan·Risk Class 1·MD·Agilent Technologies, Inc.·Registered Nov 16, 2016 – Nov 16, 2026Active

Registration details

Analysis ID: 7a8277076875edc825e89b7a4efbadab
License Form: Ministry of Health Medical Device Import No. 017180
Customs Code: DHA09401718003

Company information

Manufacturer: Agilent Technologies, Inc.
Manufacturer Country: United States
Authorized Representative: SCN TRADING COMPANY LIMITED

Product details

Intended Use: Limited to the first level identification range of immunopathological histochemical reagents and kits (B.1860) of the Measures for the Administration of Medical Devices.
Product Type (Level 1): B Hematology and pathology devices
Product Type (Level 2): B1860 Immunopathological histochemical reagents and kits
Import Information: Imported from abroad

Dates and status

Registration Date: Nov 16, 2016
Expiry Date: Nov 16, 2026

About this record

Access comprehensive regulatory information for "DAKO" Monoclonal Mouse Anti-Human PD-L1 22C3 (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 7a8277076875edc825e89b7a4efbadab and manufactured by Agilent Technologies, Inc.. The authorized representative in Taiwan is SCN TRADING COMPANY LIMITED.

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