Taiwan FDA registration 6a1d95d59fea49ac81acd233c517237c
“Arthrex” Synergy UHD4 System
TW: “艾思瑞斯”內視鏡影像系統
Taiwan·Risk Class 2·MD·ARTHREX, INC.·Registered Nov 16, 2017 – Nov 16, 2022ExpiredRegistration details
- Analysis ID
- 6a1d95d59fea49ac81acd233c517237c
- License Form
- Ministry of Health Medical Device Import No. 030556
- Customs Code
- DHA05603055605
Company information
- Manufacturer
- ARTHREX, INC.
- Manufacturer Country
- United States
- Authorized Representative
- JOINSMART BIOMEDICAL COMPANY LIMITED
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
- Nov 16, 2017
- Expiry Date
- Nov 16, 2022
About this record
Access comprehensive regulatory information for “Arthrex” Synergy UHD4 System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6a1d95d59fea49ac81acd233c517237c and manufactured by ARTHREX, INC.. The authorized representative in Taiwan is JOINSMART BIOMEDICAL COMPANY LIMITED.
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