Taiwan FDA registration 211e38119405b10ea86bc320e103c922
“Boston Scientific” Jetstream Jetwire Guidewire
TW: “波士頓科技”傑思楚導線
Taiwan·Risk Class 2·MD·Lake Region Medical·Registered Nov 07, 2016 – Nov 07, 2021CancelledRegistration details
- Analysis ID
- 211e38119405b10ea86bc320e103c922
- License Form
- Ministry of Health Medical Device Import No. 028892
- Customs Code
- DHA05602889203
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)
- E Cardiovascular devices
- Product Type (Level 2)
- E1330 Catheter Lead
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 07, 2016
- Expiry Date
- Nov 07, 2021
- Cancellation Date
- Aug 23, 2023
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for “Boston Scientific” Jetstream Jetwire Guidewire in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 211e38119405b10ea86bc320e103c922 and manufactured by Lake Region Medical. The authorized representative in Taiwan is Dutch Boston Technology Co., Ltd. Taiwan Branch.
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.
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