Taiwan FDA registration 10c17dbcf2d843de781e81b8890c7683
"AIKE" blood lancet (sterilized)
TW: "愛克" 採血針 (滅菌)
Taiwan·Risk Class 1·Qiaolian Technology Co., Ltd. Nankan No. 2 Factory·Registered Mar 21, 2017 – Mar 21, 2022CancelledRegistration details
- Analysis ID
- 10c17dbcf2d843de781e81b8890c7683
Company information
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- TAIDOC TECHNOLOGY CORPORATION
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
- 委託製造;; 國產;; QMS/QSD
Dates and status
- Registration Date
- Mar 21, 2017
- Expiry Date
- Mar 21, 2022
- Cancellation Date
- Apr 12, 2024
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "AIKE" blood lancet (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 10c17dbcf2d843de781e81b8890c7683 and manufactured by Qiaolian Technology Co., Ltd. Nankan No. 2 Factory. The authorized representative in Taiwan is TAIDOC TECHNOLOGY CORPORATION.
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