"Cardino" vacuum wound drainage sleeve (sterilized)
Taiwan·Risk Class 1·CARDINAL HEALTH, INC.·Registered Apr 11, 2006 – Apr 11, 2016Cancelled- Analysis ID
- 3de860f513b75adeeefdf93913e0e25e
- Customs Code
- DHA04400356402
- Manufacturer
- CARDINAL HEALTH, INC.
- Manufacturer Country
- United States
- Authorized Representative
- BENQ MEDICAL TECHNOLOGY CORPORATION
- Intended Use
- Limited to the first level of identification scope of "non-powered, single-patient, portable suction device (I.4680)" under the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4680 Non-motive, single patient-use, carry-on suctioning device
- Import Information
- import
- Registration Date
- Apr 11, 2006
- Expiry Date
- Apr 11, 2016
- Cancellation Date
- May 28, 2018
- Status
- Logged out
- Reason
- 許可證已逾有效期
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Access comprehensive regulatory information for "Cardino" vacuum wound drainage sleeve (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 3de860f513b75adeeefdf93913e0e25e and manufactured by CARDINAL HEALTH, INC.. The authorized representative in Taiwan is BENQ MEDICAL TECHNOLOGY CORPORATION.
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including CARDINAL HEALTH P.R. 218, INC., and 1 recent registrations in the same category. 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.