Taiwan FDA registration 8d2aed859e061d7b4eaedb3ad28026b3
"Hengxin" Schulit Safety Lancet (Sterilized)
TW: "衡欣" 舒利特安全採血針 (滅菌)
Taiwan·Risk Class 1·TIANJIN HUAHONG TECHNOLOGY CO., LTD.·Registered Mar 03, 2014 – Mar 03, 2019CancelledRegistration details
- Analysis ID
- 8d2aed859e061d7b4eaedb3ad28026b3
- Customs Code
- DHA09600208303
Company information
- Manufacturer
- TIANJIN HUAHONG TECHNOLOGY CO., LTD.
- Manufacturer Country
- 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
- QMS/QSD;; Input;; Chinese goods
Dates and status
- Registration Date
- Mar 03, 2014
- Expiry Date
- Mar 03, 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 "Hengxin" Schulit Safety 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 8d2aed859e061d7b4eaedb3ad28026b3 and manufactured by TIANJIN HUAHONG TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is Hengxin Medical Equipment Co., Ltd.
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