Taiwan FDA registration 5740b4380ac5d5bb01901f98bfce6d36
"Stryker" smooth balloon guide tube
TW: “史賽克”流暢氣球導引導管
Taiwan·Risk Class 2·Stryker Neurovascular·Registered Nov 26, 2019 – Nov 26, 2029ActiveRegistration details
- Analysis ID
- 5740b4380ac5d5bb01901f98bfce6d36
- Customs Code
- DHA05603304600
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
- Nov 26, 2019
- Expiry Date
- Nov 26, 2029
About this record
Access comprehensive regulatory information for "Stryker" smooth balloon 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 5740b4380ac5d5bb01901f98bfce6d36 and manufactured by Stryker Neurovascular. The authorized representative in Taiwan is STRYKER FAR EAST INC. TAIWAN BRANCH (USA).
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