Taiwan FDA registration 57c9c6e1986d5a10f1869a9a2a7f4f4b
"Red Electric" Lancet (Sterilization)
TW: "紅電" 採血針 (滅菌)
Taiwan·Risk Class 1·GMMC·Registered Mar 14, 2012 – Mar 14, 2017CancelledRegistration details
- Analysis ID
- 57c9c6e1986d5a10f1869a9a2a7f4f4b
- Customs Code
- DHA04401146509
Company information
- Manufacturer
- GMMC
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- Hongdian Medical Technology Co., Ltd
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Instruments for General Surgery (I.4800)".
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4800 Hand Instruments for General Surgery
- Import Information
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Mar 14, 2012
- Expiry Date
- Mar 14, 2017
- Cancellation Date
- Dec 20, 2019
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Red Electric" Lancet (Sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 57c9c6e1986d5a10f1869a9a2a7f4f4b and manufactured by GMMC. The authorized representative in Taiwan is Hongdian Medical Technology Co., Ltd.
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