“Penumbra” INDIGO Aspiration System
Taiwan·Risk Class 2·MD·Penumbra, Inc.·Registered Feb 01, 2019 – Feb 01, 2029Active- Analysis ID
- 71e91845f2d5f0ce5a49ebf3fc00ce8e
- License Form
- Ministry of Health Medical Device Import No. 032102
- Customs Code
- DHA05603210202
- Manufacturer
- Penumbra, Inc.
- Manufacturer Country
- United States
- Authorized Representative
- FRONTIER BIO-MEDICAL INC.
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular devices
- Product Type (Level 2)
- E5150 Thrombectomy catheter
- Import Information
- Imported from abroad
- Registration Date
- Feb 01, 2019
- Expiry Date
- Feb 01, 2029
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Access comprehensive regulatory information for “Penumbra” INDIGO Aspiration System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 71e91845f2d5f0ce5a49ebf3fc00ce8e and manufactured by Penumbra, Inc.. The authorized representative in Taiwan is FRONTIER BIO-MEDICAL INC..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Penumbra, Inc., and 1 recent registrations in the same category. 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.