Taiwan FDA registration 1a20a601e1b547967728c8047b56f9e9
“Penumbra” Ruby Coil System
TW: “彼娜波”瑞彼栓塞環系統
Taiwan·Risk Class 3·MD·Penumbra, Inc.·Registered May 22, 2015 – May 22, 2025ExpiredRegistration details
- Analysis ID
- 1a20a601e1b547967728c8047b56f9e9
- License Form
- Ministry of Health Medical Device Import No. 027300
- Customs Code
- DHA05602730002
Company information
- Manufacturer
- Penumbra, Inc.
- Manufacturer Country
- United States
- Authorized Representative
- FRONTIER BIO-MEDICAL INC.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular devices
- Product Type (Level 2)
- E3300 Arterial Embolization Device
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 22, 2015
- Expiry Date
- May 22, 2025
About this record
Access comprehensive regulatory information for “Penumbra” Ruby Coil System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 1a20a601e1b547967728c8047b56f9e9 and manufactured by Penumbra, Inc.. The authorized representative in Taiwan is FRONTIER BIO-MEDICAL INC..
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