Taiwan FDA registration fa5825edb6cd0df1d97ad36f362959f5
"Ndoko" catheter strapping set (sterilized)
TW: "恩多寇" 導管綁帶組 (滅菌)
Registration details
- Analysis ID
- fa5825edb6cd0df1d97ad36f362959f5
- Customs Code
- DHA09401831008
Company information
- Manufacturer
- ANDOCOR NV
- Manufacturer Country
- Belgium
- Authorized Representative
- LEIN YIH MEDICAL CO.
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Instruments for General Surgery (I.4800)".
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4800 Hand Instruments for General Surgery
- Import Information
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Sep 14, 2017
- Expiry Date
- Sep 14, 2022
- Cancellation Date
- Apr 12, 2024
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Ndoko" catheter strapping set (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number fa5825edb6cd0df1d97ad36f362959f5 and manufactured by ANDOCOR NV. The authorized representative in Taiwan is LEIN YIH MEDICAL CO..
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