Taiwan FDA registration 67dca831a205715c60502cf750d82102
“Boston Scientific” Wallstent Super Stiff Guidewire
TW: “波士頓科技”華斯登導引線
Taiwan·Risk Class 2·MD·LAKE REGION MEDICAL·Registered Jul 27, 2013 – Jul 27, 2018CancelledRegistration details
- Analysis ID
- 67dca831a205715c60502cf750d82102
- License Form
- Ministry of Health Medical Device Import No. 025305
- Customs Code
- DHA05602530502
Company information
- Manufacturer
- LAKE REGION MEDICAL
- Manufacturer Country
- United States
- Authorized Representative
- Dutch Boston Technology Co., Ltd. Taiwan Branch
Product details
- Product Type (Level 1)
- H Gastroenterology-urology devices
- Product Type (Level 2)
- H1500 endoscope and accessories
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jul 27, 2013
- Expiry Date
- Jul 27, 2018
- Cancellation Date
- Jun 22, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for “Boston Scientific” Wallstent Super Stiff Guidewire in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 67dca831a205715c60502cf750d82102 and manufactured by LAKE REGION MEDICAL. The authorized representative in Taiwan is Dutch Boston Technology Co., Ltd. Taiwan Branch.
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