Taiwan FDA registration 982ce719f2bf47a8812a0af71b218569
"Pibien" Kenle rhenium guide wire
TW: "皮必恩"肯樂錸導引導線
Taiwan·Risk Class 2·PBN MEDICALS DENMARK A/S·Registered Jul 12, 2005 – Jul 12, 2015CancelledRegistration details
- Analysis ID
- 982ce719f2bf47a8812a0af71b218569
- Customs Code
- DHA00601154105
Company information
- Manufacturer
- PBN MEDICALS DENMARK A/S
- Manufacturer Country
- Denmark
- Authorized Representative
- CHINA SPRING TRADING CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Import Information
- import
Dates and status
- Registration Date
- Jul 12, 2005
- Expiry Date
- Jul 12, 2015
- Cancellation Date
- Jun 25, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Pibien" Kenle rhenium guide wire in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 982ce719f2bf47a8812a0af71b218569 and manufactured by PBN MEDICALS DENMARK A/S. The authorized representative in Taiwan is CHINA SPRING TRADING 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