Taiwan FDA registration 5b0fa88626de086832537b93920123d5
"Rollis" blood lancet
TW: "羅利士"採血針
Registration details
- Analysis ID
- 5b0fa88626de086832537b93920123d5
- Customs Code
- DHA04600021109
Company information
- Manufacturer Country
- Canada;;China
- Authorized Representative
- U-E CHECK MEDICAL CO., LTD.
Product details
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4800 Hand Instruments for General Surgery
- Import Information
- import
Dates and status
- Registration Date
- Apr 15, 2006
- Expiry Date
- Apr 15, 2011
- Cancellation Date
- Jan 18, 2013
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Rollis" blood lancet in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 5b0fa88626de086832537b93920123d5 and manufactured by LERNAPHARM INC.;; WUXI XINDA MEDICAL DEVICE CO., LTD. The authorized representative in Taiwan is U-E CHECK MEDICAL CO., LTD..
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