Taiwan FDA registration 770faa371b88ba691b4cfc6d6d47b94e
"Joy" bone filler injection tool series (sterilization)
TW: “喜望”骨填充物注入工具系列 (滅菌)
Taiwan·Risk Class 1·SEAWON MEDITECH CO., LTD.·Registered Oct 19, 2009 – Oct 19, 2029ActiveRegistration details
- Analysis ID
- 770faa371b88ba691b4cfc6d6d47b94e
- Customs Code
- DHA04400821900
Company information
- Manufacturer
- SEAWON MEDITECH CO., LTD.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- CHEER BIOMEDICAL CORP.
Product details
- Intended Use
- Limited to the classification and grading management measures of medical equipment "Bone cement dispenser (N.4200) first level identification range.
- Product Type (Level 1)
- N Orthopedics
- Product Type (Level 2)
- N.4200 Bone cement distributor
- Import Information
- Input;; QMS/QSD
Dates and status
- Registration Date
- Oct 19, 2009
- Expiry Date
- Oct 19, 2029
About this record
Access comprehensive regulatory information for "Joy" bone filler injection tool series (sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 770faa371b88ba691b4cfc6d6d47b94e and manufactured by SEAWON MEDITECH CO., LTD.. The authorized representative in Taiwan is CHEER BIOMEDICAL 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