"Kudman" manual instruments for general surgery (unsterilized)
- Analysis ID
- be1af60c2e48df18ee4dc70027e55c10
- Customs Code
- DHA04400919300
- Manufacturer
- CODMAN & SHURTLEFF,INC.
- Manufacturer Country
- United States
- Authorized Representative
- PRO-READY ENTERPRISE CO., LTD.
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Instruments for General Surgery (I.4800)".
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4800 Hand Instruments for General Surgery
- Import Information
- import
- Registration Date
- Sep 14, 2010
- Expiry Date
- Sep 14, 2015
- Cancellation Date
- Aug 21, 2018
- Status
- Logged out
- Reason
- 未展延而逾期者
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Access comprehensive regulatory information for "Kudman" manual instruments for general surgery (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number be1af60c2e48df18ee4dc70027e55c10 and manufactured by CODMAN & SHURTLEFF,INC.. The authorized representative in Taiwan is PRO-READY ENTERPRISE CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including CODMAN & SHURTLEFF,INC., and 1 recent registrations in the same category. 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.