gudid
Primary ID: 11431532
Scenium (UDI 11431532)
Manufactured by SIEMENS MEDICAL SOLUTIONS USA, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Scenium - Primary ID 11431532
Device Regulatory Overview
The Scenium (Model/Catalog Number: 11431532) is a medical device manufactured by SIEMENS MEDICAL SOLUTIONS USA, INC.. This product is indexed under FDA Product Code / Category Classification LLZ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 11431532
- Product Code / EMDN
- LLZ
- Device Name
- Database Sync Date
- 2026-08-09 09:26:04
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Scenium?
The registered manufacturer of record for Scenium is SIEMENS MEDICAL SOLUTIONS USA, INC..
What is the Primary UDI-DI identifier for Scenium?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 11431532.
What classification code is assigned to this device?
This device is registered under product classification code LLZ.
Similar Classification Devices (LLZ)
Other Devices by SIEMENS MEDICAL SOLUTIONS USA, INC.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint