Taiwan FDA registration 52c6ca855400bfa39e0273020fd8c076
"Bud" Ike-Foss nephrostomy balloon dilation catheter
TW: “巴德” 艾克-佛斯腎造口手術氣球擴張導管
Taiwan·Risk Class 2·C.R. BARD, INC.·Registered Oct 07, 2008 – Oct 07, 2028ActiveRegistration details
- Analysis ID
- 52c6ca855400bfa39e0273020fd8c076
- Customs Code
- DHA00601925709
Company information
- Manufacturer
- C.R. BARD, INC.
- Manufacturer Country
- United States
- Authorized Representative
- BARD PACIFIC HEALTH CARE CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- H Gastroenterology and urology
- Import Information
- import
Dates and status
- Registration Date
- Oct 07, 2008
- Expiry Date
- Oct 07, 2028
About this record
Access comprehensive regulatory information for "Bud" Ike-Foss nephrostomy balloon dilation catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 52c6ca855400bfa39e0273020fd8c076 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.
Free DatabasePowered by Pure Global AI89,000+ Devices