Taiwan FDA registration 3e72db065e4255bc22b0b365d4456f5f
Amplatzer Talisman Delivery Sheath
TW: “特莉絲曼”遞送套管系統
Taiwan·Risk Class 3·MD·Abbott Medical·Registered Aug 14, 2022 – Aug 14, 2027ActiveRegistration details
- Analysis ID
- 3e72db065e4255bc22b0b365d4456f5f
- License Form
- Ministry of Health Medical Device Import No. 035754
- Customs Code
- DHA05603575408
Company information
- Manufacturer
- Abbott Medical
- Manufacturer Country
- United States
- Authorized Representative
- Abbott Medical Taiwan Co.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E1250 Percutaneous catheter
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 14, 2022
- Expiry Date
- Aug 14, 2027
About this record
Access comprehensive regulatory information for Amplatzer Talisman Delivery Sheath in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 3e72db065e4255bc22b0b365d4456f5f and manufactured by Abbott Medical. The authorized representative in Taiwan is Abbott Medical Taiwan Co..
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.
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