Taiwan FDA registration 081bf8c10265cfc0c4e943643bada610
"Pajik" balloon cannula set
TW: “帕將克”球囊套管組
Taiwan·Risk Class 2·PAJUNK GMBH MEDIZINTECHNOLOGIE·Registered Nov 24, 2009 – Nov 24, 2019CancelledRegistration details
- Analysis ID
- 081bf8c10265cfc0c4e943643bada610
- Customs Code
- DHA00602043102
Company information
- Manufacturer
- PAJUNK GMBH MEDIZINTECHNOLOGIE
- Manufacturer Country
- Germany
- Authorized Representative
- Huizhong Co., Ltd
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- H Gastroenterology and urology
- Product Type (Level 2)
- H.1500 Internal Scope and its accessories
- Import Information
- import
Dates and status
- Registration Date
- Nov 24, 2009
- Expiry Date
- Nov 24, 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 "Pajik" balloon cannula set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 081bf8c10265cfc0c4e943643bada610 and manufactured by PAJUNK GMBH MEDIZINTECHNOLOGIE. The authorized representative in Taiwan is Huizhong Co., Ltd.
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