Taiwan FDA registration 110a3744e09698f39e81a901fa3cfa2e
"Aceris" manual orthopedic surgical instruments (sterile/unsterilized)
TW: "艾思瑞斯"手動式骨科手術器械(滅菌/未滅菌)
Taiwan·Risk Class 1·ARTHREX GMBH·Registered Sep 29, 2014 – Sep 29, 2019CancelledRegistration details
- Analysis ID
- 110a3744e09698f39e81a901fa3cfa2e
- Customs Code
- DHA09401454706
Company information
- Manufacturer
- ARTHREX GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- Sinjet Limited
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
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Sep 29, 2014
- Expiry Date
- Sep 29, 2019
- Cancellation Date
- Jun 22, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Aceris" manual orthopedic surgical instruments (sterile/unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 110a3744e09698f39e81a901fa3cfa2e and manufactured by ARTHREX GMBH. The authorized representative in Taiwan is Sinjet Limited.
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