gudid
Primary ID: 053008
Kroger Insulin Syringes (UDI 053008)
Manufactured by KROGER CO., THE
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Kroger Insulin Syringes - Primary ID 053008
Device Regulatory Overview
The Kroger Insulin Syringes (Model/Catalog Number: 053008) is a medical device manufactured by KROGER CO., THE. This product is indexed under FDA Product Code / Category Classification FMF within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 053008
- Product Code / EMDN
- FMF
- Device Name
- .5cc 8mm 30G Insulin Syringe, Sterile, Single-Use, 100ct
- Database Sync Date
- 2026-08-09 09:00:34
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Kroger Insulin Syringes?
The registered manufacturer of record for Kroger Insulin Syringes is KROGER CO., THE.
What is the Primary UDI-DI identifier for Kroger Insulin Syringes?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 053008.
What classification code is assigned to this device?
This device is registered under product classification code FMF.
Similar Classification Devices (FMF)
Other Devices by KROGER CO., THE
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint