Taiwan FDA registration 19e700567b5189daf081c0bd9bcbe228
"Pinabo" Newomax system
TW: “彼娜波”紐諾邁克斯系統
Taiwan·Risk Class 2·Penumbra, Inc.·Registered May 06, 2013 – May 06, 2028ActiveRegistration details
- Analysis ID
- 19e700567b5189daf081c0bd9bcbe228
- Customs Code
- DHA00602487809
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 Medicine Science
- Product Type (Level 2)
- E.1250 Percutaneous catheters
- Import Information
- import
Dates and status
- Registration Date
- May 06, 2013
- Expiry Date
- May 06, 2028
About this record
Access comprehensive regulatory information for "Pinabo" Newomax system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 19e700567b5189daf081c0bd9bcbe228 and manufactured by Penumbra, Inc.. The authorized representative in Taiwan is FRONTIER BIO-MEDICAL INC..
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.
Free DatabasePowered by Pure Global AI89,000+ Devices