Taiwan FDA registration 33bcccf5899206d5bf58cd56e316d7a2
"Jinggang" knee compression bone plate system
TW: “精剛”膝關節壓迫性骨板系統
Taiwan·Risk Class 2·S-TECH CORP.·Registered Apr 16, 2008 – Apr 16, 2013CancelledRegistration details
- Analysis ID
- 33bcccf5899206d5bf58cd56e316d7a2
- Customs Code
- DHY00500242600
Company information
- Manufacturer
- S-TECH CORP.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- S-TECH CORP.
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
- Domestic
Dates and status
- Registration Date
- Apr 16, 2008
- Expiry Date
- Apr 16, 2013
- Cancellation Date
- Jun 03, 2015
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Jinggang" knee compression bone plate system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 33bcccf5899206d5bf58cd56e316d7a2 and manufactured by S-TECH CORP.. The authorized representative in Taiwan is S-TECH CORP..
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