Taiwan FDA registration 5c4bfcc5361a3a6778950a9e72ec58e0
Cross Manual Orthopedic Surgical Instruments (Unsterilized)
TW: 克羅斯手動式骨科手術器械(未滅菌)
Registration details
- Analysis ID
- 5c4bfcc5361a3a6778950a9e72ec58e0
- Customs Code
- DHA04400393001
Company information
- Manufacturer
- KOROS USA, INC.
- Manufacturer Country
- United States
- Authorized Representative
- FEDERAL MEDICAL CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of manual orthopedic surgical instruments (N.4540) of the Measures for the Administration of Medical Equipment.
- Product Type (Level 1)
- N Orthopedics
- Product Type (Level 2)
- N.4540 手動式骨科手術器械
- Import Information
- import
Dates and status
- Registration Date
- Apr 15, 2006
- Expiry Date
- Apr 15, 2016
- Cancellation Date
- Apr 25, 2018
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for Cross Manual Orthopedic Surgical Instruments (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 5c4bfcc5361a3a6778950a9e72ec58e0 and manufactured by KOROS USA, INC.. The authorized representative in Taiwan is FEDERAL MEDICAL 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