"Bard" non-powered wound aspiration device (sterilized)
Taiwan·Risk Class 1·HEALTH CARE PRODUCTS; C.R. BARD,INC.·Registered May 23, 2014 – May 23, 2029Active- Analysis ID
- e02292da86a17cf1c8156c3357582247
- Customs Code
- DHA09401416900
- Manufacturer
- HEALTH CARE PRODUCTS; C.R. BARD,INC.
- Manufacturer Country
- Mexico;;United States
- Authorized Representative
- BARD PACIFIC HEALTH CARE CO., LTD.
- Intended Use
- Limited to the first level of classification and grading management of medical equipment, "Non-powered, single-patient, portable suction equipment (I.4680)".
- 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
- 輸入;; 委託製造;; QMS/QSD
- Registration Date
- May 23, 2014
- Expiry Date
- May 23, 2029
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Access comprehensive regulatory information for "Bard" non-powered wound aspiration device (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e02292da86a17cf1c8156c3357582247 and manufactured by HEALTH CARE PRODUCTS; C.R. BARD,INC.. The authorized representative in Taiwan is BARD PACIFIC HEALTH CARE CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including C.R. BARD, 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.