Taiwan FDA registration 67c5409d80edf96ef3edf04174a18e09
“LDR” Mobi-C Implants
TW: “樂德爾”莫畢西頸椎植入物
Taiwan·Risk Class 2·MD·LDR MEDICAL·Registered Jun 11, 2015 – Jun 11, 2025ExpiredRegistration details
- Analysis ID
- 67c5409d80edf96ef3edf04174a18e09
- License Form
- Ministry of Health Medical Device Import No. 027419
- Customs Code
- DHA05602741901
Company information
- Manufacturer
- LDR MEDICAL
- Manufacturer Country
- France
- Authorized Representative
- ZimVie Taiwan Co., Ltd.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- N Orthopedic devices
- Product Type (Level 2)
- N3060 Spine correction fixation between vertebral bodies
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jun 11, 2015
- Expiry Date
- Jun 11, 2025
About this record
Access comprehensive regulatory information for “LDR” Mobi-C Implants in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 67c5409d80edf96ef3edf04174a18e09 and manufactured by LDR MEDICAL. The authorized representative in Taiwan is ZimVie 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