Biograph Trinion EP2 CT128 (UDI 10756479)
Manufactured by SIEMENS MEDICAL SOLUTIONS USA, INC.
Device Regulatory Overview
The Biograph Trinion EP2 CT128 (Model/Catalog Number: 10756479) is a medical device manufactured by SIEMENS MEDICAL SOLUTIONS USA, INC.. This product is indexed under FDA Product Code / Category Classification KPS within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 10756479
- Product Code / EMDN
- KPS
- Device Name
- Database Sync Date
- 2026-08-09 09:26:04
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Biograph Trinion EP2 CT128?
The registered manufacturer of record for Biograph Trinion EP2 CT128 is SIEMENS MEDICAL SOLUTIONS USA, INC..
What is the Primary UDI-DI identifier for Biograph Trinion EP2 CT128?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 10756479.
What classification code is assigned to this device?
This device is registered under product classification code KPS.
Similar Classification Devices (KPS)
Other Devices by SIEMENS MEDICAL SOLUTIONS USA, INC.
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