Taiwan FDA registration 6064e2adc61ef7818e705cb48c184e4e
Ruicheng "Beurer" Lancing Device (Non-Sterile)
TW: 瑞成 "博依" 採血筆 (未滅菌)
Taiwan·Risk Class 1·MD·BEIJING RUICHENG MEDICAL SUPPLIES CO., LTD.·Registered Jul 04, 2018 – Jul 04, 2028ActiveRegistration details
- Analysis ID
- 6064e2adc61ef7818e705cb48c184e4e
- License Form
- Ministry of Health Medical Device Land Transport No. 003476
- Customs Code
- DHA09600347601
Company information
- Manufacturer
- BEIJING RUICHENG MEDICAL SUPPLIES CO., LTD.
- Manufacturer Country
- China
- Authorized Representative
- EPS BIO TECHNOLOGY CORP.
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 and plastic surgical devices
- Product Type (Level 2)
- I4800 General Surgery Manual Instrument
- Import Information
- Imported from abroad; Made in China
Dates and status
- Registration Date
- Jul 04, 2018
- Expiry Date
- Jul 04, 2028
About this record
Access comprehensive regulatory information for Ruicheng "Beurer" Lancing Device (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 6064e2adc61ef7818e705cb48c184e4e and manufactured by BEIJING RUICHENG MEDICAL SUPPLIES CO., LTD.. The authorized representative in Taiwan is EPS BIO TECHNOLOGY CORP..
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