gudid
Primary ID: L722
EM (UDI L722)
Manufactured by Allied Medical, LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for EM - Primary ID L722
Device Regulatory Overview
The EM (Model/Catalog Number: L722) is a medical device manufactured by Allied Medical, LLC. This product is indexed under FDA Product Code / Category Classification FMR within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- L722
- Product Code / EMDN
- FMR
- Device Name
- HALFBACK ASSY
- Database Sync Date
- 2026-08-09 09:00:32
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 EM?
The registered manufacturer of record for EM is Allied Medical, LLC.
What is the Primary UDI-DI identifier for EM?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is L722.
What classification code is assigned to this device?
This device is registered under product classification code FMR.
Similar Classification Devices (FMR)
Other Devices by Allied Medical, LLC
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