gudid
Primary ID: 11007962
Symbia_Intevo_Bold (UDI 11007962)
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 Symbia_Intevo_Bold - Primary ID 11007962
Device Regulatory Overview
The Symbia_Intevo_Bold (Model/Catalog Number: 11007962) 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
- 11007962
- 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 Symbia_Intevo_Bold?
The registered manufacturer of record for Symbia_Intevo_Bold is SIEMENS MEDICAL SOLUTIONS USA, INC..
What is the Primary UDI-DI identifier for Symbia_Intevo_Bold?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 11007962.
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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