Taiwan FDA registration 9731956f8f6e280b75de25d58e268819
"Pademk" Gastroenterology-Urology Bioexamination Equipment (Sterilization)
TW: “帕將克”腸胃科-泌尿科生檢器械 (滅菌)
Taiwan·Risk Class 1·PAJUNK GMBH MEDIZINTECHNOLOGIE·Registered Jan 06, 2009 – Jan 06, 2019CancelledRegistration details
- Analysis ID
- 9731956f8f6e280b75de25d58e268819
- Customs Code
- DHA04400736809
Company information
- Manufacturer
- PAJUNK GMBH MEDIZINTECHNOLOGIE
- Manufacturer Country
- Germany
- Authorized Representative
- Huizhong Co., Ltd
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Gastroenterology-Urology Bioexamination Devices (H.1075)".
- Product Type (Level 1)
- H Gastroenterology and urology
- Product Type (Level 2)
- H.1075 腸胃科-泌尿科生檢器械
- Import Information
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Jan 06, 2009
- Expiry Date
- Jan 06, 2019
- Cancellation Date
- Aug 05, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Pademk" Gastroenterology-Urology Bioexamination Equipment (Sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9731956f8f6e280b75de25d58e268819 and manufactured by PAJUNK GMBH MEDIZINTECHNOLOGIE. The authorized representative in Taiwan is Huizhong Co., Ltd.
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