Pure Global

"Vidalik" titanium vascular clamp system - Taiwan Registration 09429d5392c7b3f705fb44ce191ae71a

Access comprehensive regulatory information for "Vidalik" titanium vascular clamp system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 09429d5392c7b3f705fb44ce191ae71a and manufactured by PETERS SURGICAL. The authorized representative in Taiwan is ASIA HEALTH CARE 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
09429d5392c7b3f705fb44ce191ae71a
Registration Details
Taiwan FDA Registration: 09429d5392c7b3f705fb44ce191ae71a
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Vidalik" titanium vascular clamp system
TW: โ€œ็ถญ้”ๅŠ›ๅ…‹โ€้ˆฆ้‡‘ๅฑฌ่ก€็ฎกๅคพ็ณป็ตฑ
Risk Class 2

Registration Details

09429d5392c7b3f705fb44ce191ae71a

DHA00602130601

Company Information

France

Product Details

For details, it is Chinese approved copy of the imitation order

I General, Plastic Surgery and Dermatology

I.4300 Implantable Clips

import

Dates and Status

Aug 10, 2010

Aug 10, 2025