gudid
Primary ID: 24-12-23
ELMED (UDI 24-12-23)
Manufactured by ELMED INCORPORATED
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ELMED - Primary ID 24-12-23
Device Regulatory Overview
The ELMED (Model/Catalog Number: 24-12-23) is a medical device manufactured by ELMED INCORPORATED. This product is indexed under FDA Product Code / Category Classification LRC within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 24-12-23
- Product Code / EMDN
- LRC
- Device Name
- RHOTON BARON 12FR., 23CM (9") SUCTION TUBE WITH FINGER CONTROL SUCTION PLATE, BULB TYPE HOSE CONNECTOR WITH .161" HOLE AND CLEARING STYLET.
- Database Sync Date
- 2026-08-09 09:13:31
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 ELMED?
The registered manufacturer of record for ELMED is ELMED INCORPORATED.
What is the Primary UDI-DI identifier for ELMED?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 24-12-23.
What classification code is assigned to this device?
This device is registered under product classification code LRC.
Similar Classification Devices (LRC)
Other Devices by ELMED INCORPORATED
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