Taiwan FDA registration d4addf733dd9bb4c0a27483e47d5cf3c
"Stryker" Constance Dome Guide Tube
TW: “史賽克”康絲翠梅絲氣球導引導管
Taiwan·Risk Class 2·Stryker Neurovascular·Registered Sep 23, 2014 – Sep 23, 2024CancelledRegistration details
- Analysis ID
- d4addf733dd9bb4c0a27483e47d5cf3c
- Customs Code
- DHA05602657000
Company information
- Manufacturer
- Stryker Neurovascular
- Manufacturer Country
- United States
- Authorized Representative
- STRYKER FAR EAST INC. TAIWAN BRANCH (USA)
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.1250 Percutaneous catheters
- Import Information
- import
Dates and status
- Registration Date
- Sep 23, 2014
- Expiry Date
- Sep 23, 2024
- Cancellation Date
- Nov 08, 2024
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for "Stryker" Constance Dome Guide Tube in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d4addf733dd9bb4c0a27483e47d5cf3c and manufactured by Stryker Neurovascular. The authorized representative in Taiwan is STRYKER FAR EAST INC. TAIWAN BRANCH (USA).
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