Low Pen HR Collimator Symbia E (UDI 10764173)
Manufactured by SIEMENS MEDICAL SOLUTIONS USA, INC.
Device Regulatory Overview
The Low Pen HR Collimator Symbia E (Model/Catalog Number: 10764173) 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
- 10764173
- Product Code / EMDN
- KPS
- Device Name
- Database Sync Date
- 2026-08-09 09:26:05
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 Low Pen HR Collimator Symbia E?
The registered manufacturer of record for Low Pen HR Collimator Symbia E is SIEMENS MEDICAL SOLUTIONS USA, INC..
What is the Primary UDI-DI identifier for Low Pen HR Collimator Symbia E?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 10764173.
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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