"Bard" non-powered wound aspiration device (sterilized) - Taiwan Registration e02292da86a17cf1c8156c3357582247
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.
Device Details
Registration Details
e02292da86a17cf1c8156c3357582247
DHA09401416900
Product Details
Limited to the first level of classification and grading management of medical equipment, "Non-powered, single-patient, portable suction equipment (I.4680)".
I General, Plastic Surgery and Dermatology
I.4680 Non-motive, single patient-use, carry-on suctioning device
่ผธๅ ฅ;; ๅง่จ่ฃฝ้ ;; QMS/QSD
Dates and Status
May 23, 2014
May 23, 2029