gudid
Primary ID: 041260369728
Kroger (UDI 041260369728)
Manufactured by KROGER CO., THE
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Kroger - Primary ID 041260369728
Device Regulatory Overview
The Kroger (Model/Catalog Number: 041260369728) is a medical device manufactured by KROGER CO., THE. This product is indexed under FDA Product Code / Category Classification LRR within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 041260369728
- Product Code / EMDN
- LRR
- Device Name
- First Aid Kit, All-Purpose First Aid Essentials, 70 items: 1 - Carrying Case, 4 - Triple Antibiotic Ointment 1/32 OZ (0.9 g); 8 - Gauze Pads 2 IN x 2 IN (50 mm x 50 mm); 5 - Antibacterial Fabric Bandages 1 IN x 3 IN (25 mm x 76 mm); 10 - Antibacterial Fabric Bandages 3/4 IN x 3 IN (19 mm x 76 mm); 15 - Antibacterial Fabric Bandages 5/8 IN x 2 1/4 IN (15 mm x 57 mm); 21 - Antibacterial Sheer Bandages 1 IN x 3 IN (25 mm x 76 mm); 6 - Hand Cleansing Wipes 4 3/4 IN x 7 3/4 IN (120 mm x 196 mm)
- Database Sync Date
- 2026-08-09 09:08:52
Full Regulatory Attributes
🔒 Token Gated
{
"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 Kroger?
The registered manufacturer of record for Kroger is KROGER CO., THE.
What is the Primary UDI-DI identifier for Kroger?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 041260369728.
What classification code is assigned to this device?
This device is registered under product classification code LRR.
Similar Classification Devices (LRR)
Other Devices by KROGER CO., THE
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