Taiwan FDA registration eca8d178b65acec6effe19e03aa2609b
“OSMD” Spinal MIS System
TW: “沃思坦”脊椎微創系統
Taiwan·Risk Class 2·MD·OSTEOSTANDARD MEDICAL DEVICE CO., LTD.·Registered Oct 29, 2018 – Oct 29, 2028ActiveRegistration details
- Analysis ID
- eca8d178b65acec6effe19e03aa2609b
- License Form
- Ministry of Health Medical Device Manufacturing No. 006192
Company information
- Manufacturer
- OSTEOSTANDARD MEDICAL DEVICE CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- OSTEOSTANDARD MEDICAL DEVICE 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)
- N3070 Pedicle screw system
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Oct 29, 2018
- Expiry Date
- Oct 29, 2028
About this record
Access comprehensive regulatory information for “OSMD” Spinal MIS System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number eca8d178b65acec6effe19e03aa2609b and manufactured by OSTEOSTANDARD MEDICAL DEVICE CO., LTD.. The authorized representative in Taiwan is OSTEOSTANDARD MEDICAL DEVICE 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