Taiwan FDA registration e2019841d4658cd9d4216c3f8e917fe2
"Hengxin" Schulit blood pen (unsterilized)
TW: “衡欣”舒利特採血筆 (未滅菌)
Taiwan·Risk Class 1·Hengxin Medical Equipment Co., Ltd·Registered May 16, 2014 – May 16, 2024CancelledRegistration details
- Analysis ID
- e2019841d4658cd9d4216c3f8e917fe2
Company information
- Manufacturer
- Hengxin Medical Equipment Co., Ltd
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Hengxin Medical Equipment 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
- Domestic
Dates and status
- Registration Date
- May 16, 2014
- Expiry Date
- May 16, 2024
- Cancellation Date
- Jun 13, 2022
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for "Hengxin" Schulit blood pen (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e2019841d4658cd9d4216c3f8e917fe2 and manufactured by Hengxin Medical Equipment Co., Ltd. The authorized representative in Taiwan is Hengxin Medical Equipment Co., Ltd.
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