"Bard" non-powered wound aspiration device (sterilized) - Taiwan Registration 5dcc888b602347ac0900f4df30e37f0a
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.
Device Details
Product Details
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.
I General, Plastic Surgery and Dermatology
I.4680 Non-motive, single patient-use, carry-on suctioning device
QMS/QSD;; ่ผธๅ ฅ
Dates and Status
Jun 03, 2008
Jun 03, 2018
Dec 20, 2019
Cancellation Information
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