gudid
Primary ID: 915-MRI
MJM 900 SERIES GURNEY (UDI 915-MRI)
Manufactured by M J M International Corporation
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for MJM 900 SERIES GURNEY - Primary ID 915-MRI
Device Regulatory Overview
The MJM 900 SERIES GURNEY (Model/Catalog Number: 915-MRI) is a medical device manufactured by M J M International Corporation. This product is indexed under FDA Product Code / Category Classification FPO within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 915-MRI
- Product Code / EMDN
- FPO
- Device Name
- Database Sync Date
- 2026-08-09 09:35:46
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 MJM 900 SERIES GURNEY?
The registered manufacturer of record for MJM 900 SERIES GURNEY is M J M International Corporation.
What is the Primary UDI-DI identifier for MJM 900 SERIES GURNEY?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 915-MRI.
What classification code is assigned to this device?
This device is registered under product classification code FPO.
Similar Classification Devices (FPO)
Other Devices by M J M International Corporation
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