"Cardino" wound drainage device (sterilization)
- Analysis ID
- b228d86ed42cb402353b2c129182f1eb
- Customs Code
- DHA04401000203
- Manufacturer
- CARDINAL HEALTH, INC.
- Manufacturer Country
- United States
- Authorized Representative
- BENQ MEDICAL TECHNOLOGY CORPORATION
- Intended Use
- Limited to the scope of Grade 1 identification of "Introduction/Drainage Catheters and Their Accessories (I.4200)" under the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4200 Incoming/Drainage Tubes and Accessories
- Import Information
- import
- Registration Date
- Mar 11, 2011
- Expiry Date
- Mar 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" wound drainage device (sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number b228d86ed42cb402353b2c129182f1eb 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, 2 companies making similar products including CARDINAL HEALTH P.R. 218, INC., CARDINAL HEALTH, INC., and 2 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.