Taiwan FDA registration 279a4182a22e105586511d531644f4f5
"Medi-Stim"VeriQ System
TW: "美得斯敦"血管流量計系統
Taiwan·Risk Class 2·MD·MediStim ASA·Registered Dec 13, 2005 – Dec 13, 2025ExpiredRegistration details
- Analysis ID
- 279a4182a22e105586511d531644f4f5
- License Form
- Department of Health Medical Device Import No. 013807
- Customs Code
- DHA00601380701
Company information
- Manufacturer
- MediStim ASA
- Manufacturer Country
- Norway
- Authorized Representative
- ANSON HEALTH CARE INC.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order.
- Product Type (Level 1)
- E Cardiovascular devices
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 13, 2005
- Expiry Date
- Dec 13, 2025
About this record
Access comprehensive regulatory information for "Medi-Stim"VeriQ System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 279a4182a22e105586511d531644f4f5 and manufactured by MediStim ASA. The authorized representative in Taiwan is ANSON HEALTH CARE INC..
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 DatabasePowered by Pure Global AI89,000+ Devices