gudid
Primary ID: 4043225
MEIJER (UDI 4043225)
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 4043225
Device Regulatory Overview
The MEIJER (Model/Catalog Number: 4043225) is a medical device manufactured by MEIJER, INC.. This product is indexed under FDA Product Code / Category Classification HHD within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 4043225
- Product Code / EMDN
- HHD
- Device Name
- REGULAR MAXIPAD WINGLESS UNSCENTED 48 CT
- 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 4043225.
What classification code is assigned to this device?
This device is registered under product classification code HHD.
Similar Classification Devices (HHD)
Other Devices by MEIJER, INC.
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