Pure Global

Vitrolife Octax Laser system - Taiwan Registration 7ca574c9329938f18a5daeaacd2b9c85

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 Database
Powered by Pure Global AI
89,000+ Devices
7ca574c9329938f18a5daeaacd2b9c85
Registration Details
Taiwan FDA Registration: 7ca574c9329938f18a5daeaacd2b9c85
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

Vitrolife Octax Laser system
TW: ๅฏ†้™€ไพ†็ฆ่ผ”ๅŠฉ็”Ÿ่‚ฒ้›ทๅฐ„็ณป็ตฑ
Risk Class 2
MD

Registration Details

7ca574c9329938f18a5daeaacd2b9c85

Ministry of Health Medical Device Import No. 033969

DHA05603396906

Company Information

Germany

Product Details

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

l Devices for obstetrics and gynecology

L6200 assisted reproductive laser system

Imported from abroad

Dates and Status

Oct 05, 2020

Oct 05, 2025