Taiwan FDA registration 1cd9a93ab623ec8e528c025ee5f01ebf
“Atricure” Manual surgical instrument for general use (Sterile)
TW: “艾翠科” 一般手術用手動式器械 (滅菌)
Taiwan·Risk Class 1·MD·Atricure, Inc.·Registered Apr 20, 2022 – Apr 20, 2027ActiveRegistration details
- Analysis ID
- 1cd9a93ab623ec8e528c025ee5f01ebf
- License Form
- Ministry of Health Medical Device Import No. 022786
- Customs Code
- DHA09402278607
Company information
- Manufacturer
- Atricure, Inc.
- Manufacturer Country
- United States
- Authorized Representative
- ASIA HEALTH CARE CO., LTD.
Product details
- Intended Use
- Limited to the first level identification scope of the "Manual Instruments for General Surgery (I.4800)" of the Measures for the Classification and Grading Management of Medical Equipment.
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I4800 General Surgery Manual Instrument
- Import Information
- Imported from abroad; GMP
Dates and status
- Registration Date
- Apr 20, 2022
- Expiry Date
- Apr 20, 2027
About this record
Access comprehensive regulatory information for “Atricure” Manual surgical instrument for general use (Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 1cd9a93ab623ec8e528c025ee5f01ebf and manufactured by Atricure, Inc.. The authorized representative in Taiwan is ASIA HEALTH CARE CO., LTD..
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