Taiwan FDA registration d43a0980c91ce1a348e506feb2b8d222
"Bioden" urine collector and its accessories (unsterilized)
TW: "百歐登" 尿液收集器及其附件 (未滅菌)
Taiwan·Risk Class 1·BIODERM INC.·Registered Mar 01, 2017 – Mar 01, 2022CancelledRegistration details
- Analysis ID
- d43a0980c91ce1a348e506feb2b8d222
- Customs Code
- DHA09401754109
Company information
- Manufacturer
- BIODERM INC.
- Manufacturer Country
- United States
- Authorized Representative
- HUILI MEDICAL EQUIPMENT LIMITED
Product details
- Intended Use
- Limited to the first level identification range of "urine collector and its accessories (H.5250)" under the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- H Gastroenterology and urology
- Product Type (Level 2)
- H.5250 Urine Collector and Accessories Thereof
- Import Information
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Mar 01, 2017
- Expiry Date
- Mar 01, 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 "Bioden" urine collector and its accessories (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d43a0980c91ce1a348e506feb2b8d222 and manufactured by BIODERM INC.. The authorized representative in Taiwan is HUILI MEDICAL EQUIPMENT LIMITED.
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