Pure Global

INNOVANCE VWF Ac - Taiwan Registration 4c9264c6e1be3ad030a8759f1f1b1d7a

Access comprehensive regulatory information for INNOVANCE VWF Ac in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4c9264c6e1be3ad030a8759f1f1b1d7a and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH. The authorized representative in Taiwan is SYSMEX TAIWAN CO., LTD..

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
4c9264c6e1be3ad030a8759f1f1b1d7a
Registration Details
Taiwan FDA Registration: 4c9264c6e1be3ad030a8759f1f1b1d7a
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

INNOVANCE VWF Ac
TW: ไผŠ่ซพๅ‡กๅธๅ‡ก่ก›ๆจ‚ๆœฌ่ฉฆๅŠ‘
Risk Class 2
MD

Registration Details

4c9264c6e1be3ad030a8759f1f1b1d7a

Ministry of Health Medical Device Import No. 033503

DHA05603350302

Company Information

Product Details

A test method for automatic detection of the activity of von Willebrand factor (VWF) in human citrate-containing plasma by particle enhancement.

B Hematology and pathology devices

Factor B7290 deficiency test

Imported from abroad

Dates and Status

Jul 10, 2020

Jul 10, 2025