Taiwan FDA registration 816b82d99da8beba50276dc1aea0cfa5
"Medtronic" craniomaxillofacial fixation system
TW: “美敦力”顱頜面固定系統
Registration details
- Analysis ID
- 816b82d99da8beba50276dc1aea0cfa5
- Customs Code
- DHA00601801404
Company information
- Manufacturer
- MEDTRONIC NEUROSURGERY
- Manufacturer Country
- United States
- Authorized Representative
- MEDTRONIC (TAIWAN) LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- N Orthopedics
- Product Type (Level 2)
- N.3030 Single or multiple metallic bone fixation devices and accessories
- Import Information
- import
Dates and status
- Registration Date
- Apr 13, 2007
- Expiry Date
- Apr 13, 2017
- Cancellation Date
- Dec 13, 2019
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Medtronic" craniomaxillofacial fixation system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 816b82d99da8beba50276dc1aea0cfa5 and manufactured by MEDTRONIC NEUROSURGERY. 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