Taiwan FDA registration 1911e38f8a8ac5c97080453e3b9ad498
“Bard” Seeker Crossing Support Catheter
TW: “巴德”喜可交叉支撐導管
Taiwan·Risk Class 2·MD·BARD PERIPHERAL VASCULAR, INC.·Registered Nov 16, 2016 – Nov 16, 2026ActiveRegistration details
- Analysis ID
- 1911e38f8a8ac5c97080453e3b9ad498
- License Form
- Ministry of Health Medical Device Import No. 029103
- Customs Code
- DHA05602910307
Company information
- Manufacturer
- BARD PERIPHERAL VASCULAR, 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)
- E Cardiovascular devices
- Product Type (Level 2)
- E1250 Percutaneous catheter
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 16, 2016
- Expiry Date
- Nov 16, 2026
About this record
Access comprehensive regulatory information for “Bard” Seeker Crossing Support Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1911e38f8a8ac5c97080453e3b9ad498 and manufactured by BARD PERIPHERAL VASCULAR, INC.. The authorized representative in Taiwan is BARD PACIFIC HEALTH CARE CO., LTD..
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