Taiwan FDA registration cb3ee99c0d523a132637464ca14f3e8f
"JOIMAX" Orthopedic manual surgical instrument (Non-Sterile)
TW: "脊美適" 手動式骨科手術器械 (未滅菌)
Registration details
- Analysis ID
- cb3ee99c0d523a132637464ca14f3e8f
- License Form
- Ministry of Health Medical Device Import No. 014886
- Customs Code
- DHA09401488602
Company information
- Manufacturer
- JOIMAX GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- LI-AN INTERNATIONAL BIOTECH CO., LTD.
Product details
- Product Type (Level 1)
- N Orthopedic devices
- Product Type (Level 2)
- N4540 Manual osteologic surgery instrument
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jan 29, 2015
- Expiry Date
- Jan 29, 2020
- Cancellation Date
- Dec 27, 2019
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for "JOIMAX" Orthopedic manual surgical instrument (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number cb3ee99c0d523a132637464ca14f3e8f and manufactured by JOIMAX GMBH. The authorized representative in Taiwan is LI-AN INTERNATIONAL 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