Taiwan FDA registration 401c2d8936aa1d2eaab36faa7622ce33
"Santomo" Manual osteologic surgery instrument (unsterilized)
TW: “三友” 手動式骨科手術器械(未滅菌)
Taiwan·Risk Class 1·Shanghai Sanyou Medical Co., Ltd.·Registered Jul 19, 2023 – Jul 19, 2028ActiveRegistration details
- Analysis ID
- 401c2d8936aa1d2eaab36faa7622ce33
- Customs Code
- DHA09600479407
Company information
- Manufacturer
- Shanghai Sanyou Medical Co., Ltd.
- Manufacturer Country
- China
- Authorized Representative
- CENTRAL MEDICAL TECHNOLOGIES INC.
Product details
- Intended Use
- Limited to the classification and grading management measures of medical equipment "Manual orthopedic surgical instruments (N.4540)" first grade identification range.
- Product Type (Level 1)
- N Orthopedics
- Product Type (Level 2)
- N.4540 手動式骨科手術器械
- Import Information
- Chinese goods;; Input;; QMS/QSD
Dates and status
- Registration Date
- Jul 19, 2023
- Expiry Date
- Jul 19, 2028
About this record
Access comprehensive regulatory information for "Santomo" Manual osteologic surgery instrument (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 401c2d8936aa1d2eaab36faa7622ce33 and manufactured by Shanghai Sanyou Medical Co., Ltd.. The authorized representative in Taiwan is CENTRAL MEDICAL TECHNOLOGIES INC..
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