"Bard" Ike-Foss balloon expansion catheter - Taiwan Registration 03863bae680f8aa7e0b6c48ad233394b
Access comprehensive regulatory information for "Bard" Ike-Foss balloon expansion catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 03863bae680f8aa7e0b6c48ad233394b 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. 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
For details, it is Chinese approved copy of the imitation order
H Gastroenterology and urology
H.5470 ่ผธๅฐฟ็ฎกๆดๅผตๅจ
import
Dates and Status
Oct 24, 2008
Oct 24, 2018
May 19, 2022
Cancellation Information
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