Taiwan FDA registration 7ca574c9329938f18a5daeaacd2b9c85
Vitrolife Octax Laser system
TW: 密陀來福輔助生育雷射系統
Taiwan·Risk Class 2·MD·VITROLIFE GMBH·Registered Oct 05, 2020 – Oct 05, 2025ExpiredRegistration details
- Analysis ID
- 7ca574c9329938f18a5daeaacd2b9c85
- License Form
- Ministry of Health Medical Device Import No. 033969
- Customs Code
- DHA05603396906
Company information
- Manufacturer
- VITROLIFE GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- TSENG HSIANG LIFE SCIENCE LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- l Devices for obstetrics and gynecology
- Product Type (Level 2)
- L6200 assisted reproductive laser system
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 05, 2020
- Expiry Date
- Oct 05, 2025
About this record
Access comprehensive regulatory information for Vitrolife Octax Laser system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7ca574c9329938f18a5daeaacd2b9c85 and manufactured by VITROLIFE GMBH. The authorized representative in Taiwan is TSENG HSIANG LIFE SCIENCE 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