Taiwan FDA registration 31e2b56a58dfe15f3bfc17434ff5984c
"Pinabo" INTICO suction system
TW: “彼娜波”英迪高抽吸系統
Taiwan·Risk Class 2·Penumbra, Inc.·Registered Dec 14, 2022 – Dec 14, 2027ActiveRegistration details
- Analysis ID
- 31e2b56a58dfe15f3bfc17434ff5984c
- Customs Code
- DHA05603606401
Company information
- Manufacturer
- Penumbra, Inc.
- Manufacturer Country
- United States
- Authorized Representative
- FRONTIER BIO-MEDICAL 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.5150 血栓切除術導管
- Import Information
- import
Dates and status
- Registration Date
- Dec 14, 2022
- Expiry Date
- Dec 14, 2027
About this record
Access comprehensive regulatory information for "Pinabo" INTICO suction system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 31e2b56a58dfe15f3bfc17434ff5984c and manufactured by Penumbra, Inc.. The authorized representative in Taiwan is FRONTIER BIO-MEDICAL INC..
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