Taiwan FDA registration 0449aab91e1956167d3526c5e9d699ab
"Sunover" waste collection bag (unsterilized)
TW: "日溢" 廢液收集袋 (未滅菌)
Taiwan·Risk Class 1·HISPA MEDICAL & EQUIPMENT(GZ) CO., LTD·Registered Dec 25, 2013 – Dec 25, 2018CancelledRegistration details
- Analysis ID
- 0449aab91e1956167d3526c5e9d699ab
- Customs Code
- DHA09600204406
Company information
- Manufacturer
- HISPA MEDICAL & EQUIPMENT(GZ) CO., LTD
- Manufacturer Country
- China
- Authorized Representative
- Sunray Health Limited
Product details
- Intended Use
- Limited to the first level of identification scope of "non-powered, single-patient, portable suction device (I.4680)" under the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4680 Non-motive, single patient-use, carry-on suctioning device
- Import Information
- Chinese goods;; input
Dates and status
- Registration Date
- Dec 25, 2013
- Expiry Date
- Dec 25, 2018
- Cancellation Date
- Jul 15, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Sunover" waste collection bag (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 0449aab91e1956167d3526c5e9d699ab and manufactured by HISPA MEDICAL & EQUIPMENT(GZ) CO., LTD. The authorized representative in Taiwan is Sunray Health Limited.
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