Taiwan FDA registration a0c23032e831e99985d9d5dd05647c0d
“SIGNUS” MOBIS II ST Spinal Implant
TW: “席奈斯”模比斯多孔鈦金屬腰椎植入物
Taiwan·Risk Class 2·MD·SIGNUS Medizintechnik GmbH·Registered May 09, 2020 – May 09, 2025ExpiredRegistration details
- Analysis ID
- a0c23032e831e99985d9d5dd05647c0d
- License Form
- Ministry of Health Medical Device Import No. 033633
- Customs Code
- DHA05603363302
Company information
- Manufacturer
- SIGNUS Medizintechnik GmbH
- Manufacturer Country
- Germany
- Authorized Representative
- LI MIN BIOTECH 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)
- N3080 Interbody fusion device
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 09, 2020
- Expiry Date
- May 09, 2025
About this record
Access comprehensive regulatory information for “SIGNUS” MOBIS II ST Spinal Implant in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a0c23032e831e99985d9d5dd05647c0d and manufactured by SIGNUS Medizintechnik GmbH. The authorized representative in Taiwan is LI MIN BIOTECH 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