gudid
Primary ID: 7252
CONTOUR NEXT EZ (UDI 7252)
Manufactured by ASCENSIA DIABETES CARE US INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CONTOUR NEXT EZ - Primary ID 7252
Device Regulatory Overview
The CONTOUR NEXT EZ (Model/Catalog Number: 7252) is a medical device manufactured by ASCENSIA DIABETES CARE US INC.. This product is indexed under FDA Product Code / Category Classification LFR within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 7252
- Product Code / EMDN
- LFR
- Device Name
- Blood Glucose Monitoring System. 1 kit. For self-testing, monitoring and management of blood glucose.This kit contains the following items: CONTOUR Next EZ Blood Glucose Meter; User Guide; Quick Reference Guide; Lancing Device; 10 Colored Lancets (provided sterile); Logbook; Carrying Case.
- Database Sync Date
- 2026-08-09 09:20:16
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 CONTOUR NEXT EZ?
The registered manufacturer of record for CONTOUR NEXT EZ is ASCENSIA DIABETES CARE US INC..
What is the Primary UDI-DI identifier for CONTOUR NEXT EZ?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 7252.
What classification code is assigned to this device?
This device is registered under product classification code LFR.
Similar Classification Devices (LFR)
Other Devices by ASCENSIA DIABETES CARE US INC.
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