"Bard" non-powered wound aspiration device (sterilized)
Taiwan·Risk Class 1·C.R. BARD, INC.·Registered Jun 03, 2008 – Jun 03, 2018Cancelled- Analysis ID
- 5dcc888b602347ac0900f4df30e37f0a
- Customs Code
- DHA04400678303
- Manufacturer
- C.R. BARD, INC.
- Manufacturer Country
- United States
- Authorized Representative
- BARD PACIFIC HEALTH CARE CO., LTD.
- 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
- QMS/QSD;; 輸入
- Registration Date
- Jun 03, 2008
- Expiry Date
- Jun 03, 2018
- Cancellation Date
- Dec 20, 2019
- Status
- Logged out
- Reason
- 未展延而逾期者
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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 5dcc888b602347ac0900f4df30e37f0a and manufactured by 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 HEALTH CARE PRODUCTS; 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.