gudid
Primary ID: 930
MJM 900 SERIES GURNEY (UDI 930)
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 930
Device Regulatory Overview
The MJM 900 SERIES GURNEY (Model/Catalog Number: 930) 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
- 930
- 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 930.
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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