Taiwan FDA registration d950eae732bc7cda9e89bb2b550eabbc
"Qingying" lavage syringe (unsterilized)
TW: “晴英”灌洗注射筒 (未滅菌)
Taiwan·Risk Class 1·GENESIS BIOSYSTEMS, INC.·Registered Aug 24, 2012 – Aug 24, 2022CancelledRegistration details
- Analysis ID
- d950eae732bc7cda9e89bb2b550eabbc
- Customs Code
- DHA04401209800
Company information
- Manufacturer
- GENESIS BIOSYSTEMS, INC.
- Manufacturer Country
- United States
- Authorized Representative
- Wo Medical Limited
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Lavage Syringe (J.6960)".
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.6960 Lavage syringe
- Import Information
- import
Dates and status
- Registration Date
- Aug 24, 2012
- Expiry Date
- Aug 24, 2022
- Cancellation Date
- Apr 12, 2024
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Qingying" lavage syringe (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d950eae732bc7cda9e89bb2b550eabbc and manufactured by GENESIS BIOSYSTEMS, INC.. The authorized representative in Taiwan is Wo Medical Limited.
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