Taiwan FDA registration e44951d5a57d5e76c2eaca4c599d835c
"Cardinal" Wound Drainage Devices (Non-Sterile)
TW: "卡迪諾" 傷口引流裝置 (未滅菌)
Taiwan·Risk Class 1·MD·CARDINAL HEALTH·Registered Nov 18, 2015 – Nov 18, 2020CancelledRegistration details
- Analysis ID
- e44951d5a57d5e76c2eaca4c599d835c
- License Form
- Ministry of Health Medical Device Import No. 015871
- Customs Code
- DHA09401587107
Company information
- Manufacturer
- CARDINAL HEALTH
- Manufacturer Country
- United States
- Authorized Representative
- BENQ MEDICAL TECHNOLOGY CORPORATION
Product details
- Product Type (Level 1)
- I General and plastic surgical devices
- Product Type (Level 2)
- I4200 Introduction/drainage catheters and their accessories
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 18, 2015
- Expiry Date
- Nov 18, 2020
- Cancellation Date
- Jun 16, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期未申請展延
About this record
Access comprehensive regulatory information for "Cardinal" Wound Drainage Devices (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 e44951d5a57d5e76c2eaca4c599d835c and manufactured by CARDINAL HEALTH. The authorized representative in Taiwan is BENQ MEDICAL TECHNOLOGY CORPORATION.
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