Taiwan FDA registration 09429d5392c7b3f705fb44ce191ae71a
"Vidalik" titanium vascular clamp system
TW: “維達力克”鈦金屬血管夾系統
Registration details
- Analysis ID
- 09429d5392c7b3f705fb44ce191ae71a
- Customs Code
- DHA00602130601
Company information
- Manufacturer
- PETERS SURGICAL
- Manufacturer Country
- France
- Authorized Representative
- ASIA HEALTH CARE CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4300 Implantable Clips
- Import Information
- import
Dates and status
- Registration Date
- Aug 10, 2010
- Expiry Date
- Aug 10, 2025
About this record
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 DatabasePowered by Pure Global AI89,000+ Devices