eudamed_udi
Primary ID: 04262421840023
SQOOM medical (UDI 04262421840023)
Manufactured by Bionmed Technologies GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SQOOM medical - Primary ID 04262421840023
Device Regulatory Overview
The SQOOM medical (Model/Catalog Number: 10100) is a medical device manufactured by Bionmed Technologies GmbH. This product is indexed under FDA Product Code / Category Classification V9011 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 10100
- Product Code / EMDN
- V9011
- Device Name
- BionMed clinical Ultraschallsystem
- Database Sync Date
- 2026-08-09 16:58:36
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 SQOOM medical?
The registered manufacturer of record for SQOOM medical is Bionmed Technologies GmbH.
What is the Primary UDI-DI identifier for SQOOM medical?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04262421840023.
What classification code is assigned to this device?
This device is registered under product classification code V9011.
Similar Classification Devices (V9011)
Other Devices by Bionmed Technologies GmbH
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