Taiwan FDA registration 79dbf3b7fc84d3afc94f48aa893468ae
Stellans Boi lancet (sterilized)
TW: 施德蘭斯 博依 採血針(滅菌)
Taiwan·Risk Class 1·SteriLance Medical (Suzhou) Inc.·Registered Jan 10, 2024 – Jan 10, 2029ActiveRegistration details
- Analysis ID
- 79dbf3b7fc84d3afc94f48aa893468ae
- Customs Code
- DHA09600486902
Company information
- Manufacturer
- SteriLance Medical (Suzhou) Inc.
- Manufacturer Country
- China
- Authorized Representative
- EPS BIO TECHNOLOGY CORP.
Product details
- Intended Use
- Limited to the first level identification scope of the "Manual Instruments for General Surgery (I.4800)" of the Measures for the Classification and Grading Management of Medical Equipment.
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4800 Hand Instruments for General Surgery
- Import Information
- Input;; QMS/QSD;; Chinese goods
Dates and status
- Registration Date
- Jan 10, 2024
- Expiry Date
- Jan 10, 2029
About this record
Access comprehensive regulatory information for Stellans Boi 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 79dbf3b7fc84d3afc94f48aa893468ae and manufactured by SteriLance Medical (Suzhou) Inc.. The authorized representative in Taiwan is EPS BIO TECHNOLOGY CORP..
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