Taiwan FDA registration a97b914c5640b6e7a30580f0cde40435
Schbir blood lancet
TW: 施比爾採血針
Taiwan·Risk Class 1·SUZHOU SPR MEDICAL DEVICES DEVELOPMENT CO., LTD.·Registered Jan 10, 2006 – Jan 10, 2011CancelledRegistration details
- Analysis ID
- a97b914c5640b6e7a30580f0cde40435
- Customs Code
- DHA04600009303
Company information
- Manufacturer
- SUZHOU SPR MEDICAL DEVICES DEVELOPMENT CO., LTD.
- Manufacturer Country
- China
- Authorized Representative
- BIONIME CORPORATION
Product details
- Intended Use
- The skin is punctured and a small blood sample is collected.
- 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
- Jan 10, 2006
- Expiry Date
- Jan 10, 2011
- Cancellation Date
- Oct 29, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Schbir 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 a97b914c5640b6e7a30580f0cde40435 and manufactured by SUZHOU SPR MEDICAL DEVICES DEVELOPMENT CO., LTD.. The authorized representative in Taiwan is BIONIME CORPORATION.
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