gudid
Primary ID: OM 59-0125
ORTHOMED (UDI OM 59-0125)
Manufactured by ORTHO-MED, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ORTHOMED - Primary ID OM 59-0125
Device Regulatory Overview
The ORTHOMED (Model/Catalog Number: OM 59-0125) is a medical device manufactured by ORTHO-MED, INC.. This product is indexed under FDA Product Code / Category Classification LRY within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- OM 59-0125
- Product Code / EMDN
- LRY
- Device Name
- FS KERRISON RONGEUR TFP 5MM X 15MM 8" 40 DEGREE
- Database Sync Date
- 2026-08-09 09:06:25
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 ORTHOMED?
The registered manufacturer of record for ORTHOMED is ORTHO-MED, INC..
What is the Primary UDI-DI identifier for ORTHOMED?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is OM 59-0125.
What classification code is assigned to this device?
This device is registered under product classification code LRY.
Similar Classification Devices (LRY)
Other Devices by ORTHO-MED, INC.
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