Taiwan FDA registration 09cb1e54d721f900384cf424d634c499
“Zimmer” NavitrackER Reference Marker Device
TW: “捷邁”導航標記裝置
Taiwan·Risk Class 2·MD·ZIMMER CAS·Registered May 28, 2021 – May 28, 2026ExpiredRegistration details
- Analysis ID
- 09cb1e54d721f900384cf424d634c499
- License Form
- Ministry of Health Medical Device Import No. 034576
- Customs Code
- DHA05603457605
Company information
- Manufacturer
- ZIMMER CAS
- Manufacturer Country
- Canada
- Authorized Representative
- ZIMMER BIOMET TAIWAN CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- K Devices for neuroscience
- Product Type (Level 2)
- K4560 Instrument for stereotaxic use in the nervous system
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 28, 2021
- Expiry Date
- May 28, 2026
About this record
Access comprehensive regulatory information for “Zimmer” NavitrackER Reference Marker Device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 09cb1e54d721f900384cf424d634c499 and manufactured by ZIMMER CAS. The authorized representative in Taiwan is ZIMMER BIOMET TAIWAN CO., 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