Taiwan FDA registration 53fc9e7cbbd9925ebf2692f19bb9cc20
"Puyi" diagnostic X-ray tube sleeve assembly (unsterilized)
TW: "普一" 診斷用X光球管套組件 (未滅菌)
Taiwan·Risk Class 1·PO YE X-RAY MFG. CORP.·Registered Aug 14, 2014 – Aug 14, 2024ExpiredRegistration details
- Analysis ID
- 53fc9e7cbbd9925ebf2692f19bb9cc20
Company information
- Manufacturer
- PO YE X-RAY MFG. CORP.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- PO YE X-RAY MFG. CORP.
Product details
- Intended Use
- Limited to the first level identification range of the "X-ray tube sleeve assembly for diagnosis (P.1760)" of the Measures for the Classification and Grading Management of Medical Equipment.
- Product Type (Level 1)
- P Radiology Science
- Product Type (Level 2)
- P.1760 診斷用X光球管套組件
- Import Information
- Domestic
Dates and status
- Registration Date
- Aug 14, 2014
- Expiry Date
- Aug 14, 2024
About this record
Access comprehensive regulatory information for "Puyi" diagnostic X-ray tube sleeve assembly (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 53fc9e7cbbd9925ebf2692f19bb9cc20 and manufactured by PO YE X-RAY MFG. CORP.. The authorized representative in Taiwan is PO YE X-RAY MFG. CORP..
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