Pure Global

"Leica" Bond Ready-to-Use Primary Antibody Cytokeratin 20 (Ks20.8) (Non-Sterile) - Taiwan Registration 698d4fe8a3b1eaffe9ff180936557fc9

Access comprehensive regulatory information for "Leica" Bond Ready-to-Use Primary Antibody Cytokeratin 20 (Ks20.8) (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 698d4fe8a3b1eaffe9ff180936557fc9 and manufactured by LEICA BIOSYSTEMS NEWCASTLE LTD.. The authorized representative in Taiwan is BECKMAN COULTER TAIWAN INC., TAIWAN BRANCH (U.S.A.).

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.

Free Database
Powered by Pure Global AI
89,000+ Devices
698d4fe8a3b1eaffe9ff180936557fc9
Registration Details
Taiwan FDA Registration: 698d4fe8a3b1eaffe9ff180936557fc9
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Leica" Bond Ready-to-Use Primary Antibody Cytokeratin 20 (Ks20.8) (Non-Sterile)
TW: โ€œ้Œธๅกโ€้‚ฆๅพทๅณ็”จๅž‹็ดฐ่ƒž่ง’่ณช่›‹็™ฝ20ไธ€็ดšๆŠ—้ซ”(Ks20.8) (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

698d4fe8a3b1eaffe9ff180936557fc9

Ministry of Health Medical Device Import No. 020252

DHA09402025202

Company Information

Product Details

Limited to the first level identification range of immunopathological histochemical reagents and kits (B.1860) of the Measures for the Administration of Medical Devices.

B Hematology and pathology devices

B1860 Immunopathological histochemical reagents and kits

Imported from abroad

Dates and Status

Mar 29, 2019

Mar 29, 2024