Taiwan FDA registration 564498ddbb0b998f5b52e8b58dc0f90b
"Esres" half-moon cartilage suture repairer
TW: “艾思瑞斯”半月軟骨縫合修補器
Taiwan·Risk Class 2·ARTHREX INC.·Registered Sep 21, 2009 – Sep 21, 2024ExpiredRegistration details
- Analysis ID
- 564498ddbb0b998f5b52e8b58dc0f90b
- Customs Code
- DHA00602018701
Company information
- Manufacturer
- ARTHREX INC.
- Manufacturer Country
- United States
- Authorized Representative
- JOINSMART BIOMEDICAL COMPANY LIMITED
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.5000 Non-absorbable polyethylene terephthalate sewing wire
- Import Information
- import
Dates and status
- Registration Date
- Sep 21, 2009
- Expiry Date
- Sep 21, 2024
About this record
Access comprehensive regulatory information for "Esres" half-moon cartilage suture repairer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 564498ddbb0b998f5b52e8b58dc0f90b and manufactured by ARTHREX INC.. The authorized representative in Taiwan is JOINSMART BIOMEDICAL COMPANY LIMITED.
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