Taiwan FDA registration 3b4a1897a7558344fd9204e0b565c56a
“Quest” Artemis Handheld System
TW: “奎斯特”阿蒂蜜絲手術用內視鏡系統
Taiwan·Risk Class 2·MD·Quest Medical Imaging·Registered Feb 17, 2017 – Feb 17, 2022ExpiredRegistration details
- Analysis ID
- 3b4a1897a7558344fd9204e0b565c56a
- License Form
- Ministry of Health Medical Device Import No. 029391
- Customs Code
- DHA05602939102
Company information
- Manufacturer
- Quest Medical Imaging
- Manufacturer Country
- Netherlands
- Authorized Representative
- Yuanyou Industrial Co., Ltd
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- H Gastroenterology-urology devices
- Product Type (Level 2)
- H1500 endoscope and accessories
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Feb 17, 2017
- Expiry Date
- Feb 17, 2022
About this record
Access comprehensive regulatory information for “Quest” Artemis Handheld System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3b4a1897a7558344fd9204e0b565c56a and manufactured by Quest Medical Imaging. The authorized representative in Taiwan is Yuanyou Industrial 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