Taiwan FDA registration 28050d2f7cad13b647247d67f7c248b4
"Acerys" double-tube syringe system
TW: “艾思瑞斯”雙管注射器系統
Taiwan·Risk Class 2·TRANSCOJECT GMBH;; Arthrex, Inc.·Registered Jan 08, 2015 – Jan 08, 2030ActiveRegistration details
- Analysis ID
- 28050d2f7cad13b647247d67f7c248b4
- Customs Code
- DHA05602690604
Company information
- Manufacturer
- TRANSCOJECT GMBH;; Arthrex, Inc.
- Manufacturer Country
- United States;;Germany
- 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)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.5860 活塞式注射筒
- Import Information
- import
Dates and status
- Registration Date
- Jan 08, 2015
- Expiry Date
- Jan 08, 2030
About this record
Access comprehensive regulatory information for "Acerys" double-tube syringe system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 28050d2f7cad13b647247d67f7c248b4 and manufactured by TRANSCOJECT GMBH;; Arthrex, Inc.. The authorized representative in Taiwan is JOINSMART BIOMEDICAL COMPANY LIMITED.
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