Taiwan FDA registration 9742a17fc0d8486c20f660bc604a478e
"Okutai" plugging propeller
TW: “奧庫泰”封堵器推進器
Taiwan·Risk Class 2·Occlutech GmbH·Registered Nov 25, 2022 – Nov 25, 2027ActiveRegistration details
- Analysis ID
- 9742a17fc0d8486c20f660bc604a478e
- Customs Code
- DHA05603605704
Company information
- Manufacturer
- Occlutech GmbH
- Manufacturer Country
- Germany
- Authorized Representative
- MEDICARE UNITECH INC.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- 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 25, 2022
- Expiry Date
- Nov 25, 2027
About this record
Access comprehensive regulatory information for "Okutai" plugging propeller in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9742a17fc0d8486c20f660bc604a478e and manufactured by Occlutech GmbH. The authorized representative in Taiwan is MEDICARE UNITECH INC..
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