Taiwan FDA registration 685ca197e4eafe0e3bdfe101e06577a1
"Caudis" Pipery expander
TW: "考迪斯" 派利擴張器
Registration details
- Analysis ID
- 685ca197e4eafe0e3bdfe101e06577a1
- Customs Code
- DHA00601015202
Company information
- Manufacturer
- BIOSENSE WEBSTER, INC.
- Manufacturer Country
- United States
- Authorized Representative
- JOHNSON & JOHNSON MEDICAL TAIWAN LTD.
Product details
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Import Information
- import
Dates and status
- Registration Date
- Dec 18, 2002
- Expiry Date
- Dec 18, 2017
- Cancellation Date
- Nov 04, 2019
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Caudis" Pipery expander in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 685ca197e4eafe0e3bdfe101e06577a1 and manufactured by BIOSENSE WEBSTER, INC.. The authorized representative in Taiwan is JOHNSON & JOHNSON MEDICAL TAIWAN 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