LEAP Collimator Asm Symbia (UDI 07331882)
Manufactured by SIEMENS MEDICAL SOLUTIONS USA, INC.
Device Regulatory Overview
The LEAP Collimator Asm Symbia (Model/Catalog Number: 07331882) 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
- 07331882
- 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 LEAP Collimator Asm Symbia?
The registered manufacturer of record for LEAP Collimator Asm Symbia is SIEMENS MEDICAL SOLUTIONS USA, INC..
What is the Primary UDI-DI identifier for LEAP Collimator Asm Symbia?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07331882.
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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