SOMATOM Pro.Pulse (UDI 04056869973500)
Manufactured by Siemens Shanghai Medical Equipment Ltd.
Device Regulatory Overview
The SOMATOM Pro.Pulse (Model/Catalog Number: 11594788) is a medical device manufactured by Siemens Shanghai Medical Equipment Ltd.. This product is indexed under FDA Product Code / Category Classification Z11030605 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 11594788
- Product Code / EMDN
- Z11030605
- Device Name
- SOMATOM CT-Scanner_SHA NH
- Database Sync Date
- 2026-08-09 16:46:31
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 SOMATOM Pro.Pulse?
The registered manufacturer of record for SOMATOM Pro.Pulse is Siemens Shanghai Medical Equipment Ltd..
What is the Primary UDI-DI identifier for SOMATOM Pro.Pulse?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04056869973500.
What classification code is assigned to this device?
This device is registered under product classification code Z11030605.
Similar Classification Devices (Z11030605)
Other Devices by Siemens Shanghai Medical Equipment Ltd.
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