Taiwan FDA registration 45111ddbb307633e1dab1ccaeff5e4a0
Suzhou Schbier blood pen
TW: 蘇州施比爾採血筆
Taiwan·Risk Class 1·SUZHOU SPR MEDICAL DEVICES DEVELOPMENT CO., LTD.·Registered Jun 06, 2007 – Jun 06, 2012CancelledRegistration details
- Analysis ID
- 45111ddbb307633e1dab1ccaeff5e4a0
- Customs Code
- DHA04600038901
Company information
- Manufacturer
- SUZHOU SPR MEDICAL DEVICES DEVELOPMENT CO., LTD.
- Manufacturer Country
- China
- Authorized Representative
- Huisheng Technology 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
- Input;; Chinese goods
Dates and status
- Registration Date
- Jun 06, 2007
- Expiry Date
- Jun 06, 2012
- Cancellation Date
- May 05, 2014
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Suzhou Schbier blood pen in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 45111ddbb307633e1dab1ccaeff5e4a0 and manufactured by SUZHOU SPR MEDICAL DEVICES DEVELOPMENT CO., LTD.. The authorized representative in Taiwan is Huisheng Technology Co., Ltd.
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices