Taiwan FDA registration 27a752e706a0b3318e076d4fc334aba7
"Medtronic" Pyromi titanium bone mesh system
TW: "美敦力" 派羅米鈦質骨網系統
Taiwan·Risk Class 2·MEDTRONIC SOFAMOR DANEK MANUFACTURING·Registered Sep 03, 2003 – Sep 03, 2023ExpiredRegistration details
- Analysis ID
- 27a752e706a0b3318e076d4fc334aba7
- Customs Code
- DHA00601038907
Company information
- Manufacturer
- MEDTRONIC SOFAMOR DANEK MANUFACTURING
- Manufacturer Country
- United States
- Authorized Representative
- MEDTRONIC (TAIWAN) LTD.
Product details
- Product Type (Level 1)
- N Orthopedics
- Import Information
- import
Dates and status
- Registration Date
- Sep 03, 2003
- Expiry Date
- Sep 03, 2023
About this record
Access comprehensive regulatory information for "Medtronic" Pyromi titanium bone mesh system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 27a752e706a0b3318e076d4fc334aba7 and manufactured by MEDTRONIC SOFAMOR DANEK MANUFACTURING. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
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