Taiwan FDA registration f7da2757f6bdac26a2350f42be369665
"Puyi" mobile X-ray system
TW: "普一" 移動式X光系統
Registration details
- Analysis ID
- f7da2757f6bdac26a2350f42be369665
- Customs Code
- DHY00500107801
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
- Product Type (Level 1)
- P Radiology Science
- Import Information
- Domestic
Dates and status
- Registration Date
- Feb 20, 2004
- Expiry Date
- Feb 20, 2029
About this record
Access comprehensive regulatory information for "Puyi" mobile X-ray system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f7da2757f6bdac26a2350f42be369665 and manufactured by PO YE X-RAY MFG. CORP.. The authorized representative in Taiwan is PO YE X-RAY MFG. CORP..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
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