Taiwan FDA registration dfc5821f2b911f1d690ca5c971325d7a
“Endo Vision” Spinal Endoscopic Instruments (Non-sterile)
TW: “安德順”脊椎內視鏡工具(未滅菌)
Taiwan·Risk Class 1·MD·Endo Vision，Inc·Registered Feb 26, 2019 – Feb 26, 2024ExpiredRegistration details
- Analysis ID
- dfc5821f2b911f1d690ca5c971325d7a
- License Form
- Ministry of Health Medical Device Import No. 020130
- Customs Code
- DHA09402013001
Company information
- Manufacturer
- Endo Vision，Inc
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- EUROPE ROYAL MEDICAL DEVICES INDUSTRIAL CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of "Arthroscopy (N.1100)" of the Measures for the Administration of Medical Equipment.
- Product Type (Level 1)
- N Orthopedic devices
- Product Type (Level 2)
- N1100 Arthroscopy
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Feb 26, 2019
- Expiry Date
- Feb 26, 2024
About this record
Access comprehensive regulatory information for “Endo Vision” Spinal Endoscopic Instruments (Non-sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number dfc5821f2b911f1d690ca5c971325d7a and manufactured by Endo Vision，Inc. The authorized representative in Taiwan is EUROPE ROYAL MEDICAL DEVICES INDUSTRIAL CO., LTD..
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