Taiwan FDA registration 1cd58b754f1ab7d5b697fed1ddf51058
"Medtronic" double-lumen catheter and vascular puncture group
TW: “美敦力” 雙腔導管及血管穿刺組
Taiwan·Risk Class 2·MC3 Inc.·Registered Oct 23, 2024 – Oct 23, 2029ActiveRegistration details
- Analysis ID
- 1cd58b754f1ab7d5b697fed1ddf51058
- Customs Code
- DHA05603743604
Company information
- Manufacturer
- MC3 Inc.
- Manufacturer Country
- United States
- Authorized Representative
- MEDTRONIC (TAIWAN) LTD.
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.4100 Long-term respiration/cardiopulmonary insufficiency
- Import Information
- import
Dates and status
- Registration Date
- Oct 23, 2024
- Expiry Date
- Oct 23, 2029
About this record
Access comprehensive regulatory information for "Medtronic" double-lumen catheter and vascular puncture group in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1cd58b754f1ab7d5b697fed1ddf51058 and manufactured by MC3 Inc.. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
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