gudid
Primary ID: 7792
Meijer (UDI 7792)
Manufactured by MEIJER, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Meijer - Primary ID 7792
Device Regulatory Overview
The Meijer (Model/Catalog Number: 7792) is a medical device manufactured by MEIJER, INC.. This product is indexed under FDA Product Code / Category Classification FQH within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 7792
- Product Code / EMDN
- FQH
- Device Name
- Sterile Saline Wound Wash. Packaged in an Aerosol (BOV) can.
- Database Sync Date
- 2026-08-09 09:04:13
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 Meijer?
The registered manufacturer of record for Meijer is MEIJER, INC..
What is the Primary UDI-DI identifier for Meijer?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 7792.
What classification code is assigned to this device?
This device is registered under product classification code FQH.
Similar Classification Devices (FQH)
Other Devices by MEIJER, INC.
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