gudid
Primary ID: 7917
CONTOUR NEXT GEN (UDI 7917)
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 GEN - Primary ID 7917
Device Regulatory Overview
The CONTOUR NEXT GEN (Model/Catalog Number: 7917) is a medical device manufactured by ASCENSIA DIABETES CARE US INC.. This product is indexed under FDA Product Code / Category Classification NBW within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 7917
- Product Code / EMDN
- NBW
- Device Name
- Blood Glucose Monitoring System. 1 kit. For self-testing, monitoring and management of blood glucose.Kit contains: CONTOUR NEXT GEN blood glucose meter, Lancing Device, 10 MICROLET lancets, User Guide, Quick Reference Guide, Carrying Case, Web Registration/Warranty Card.
- Database Sync Date
- 2026-08-09 09:20:15
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 CONTOUR NEXT GEN?
The registered manufacturer of record for CONTOUR NEXT GEN is ASCENSIA DIABETES CARE US INC..
What is the Primary UDI-DI identifier for CONTOUR NEXT GEN?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 7917.
What classification code is assigned to this device?
This device is registered under product classification code NBW.
Similar Classification Devices (NBW)
Other Devices by ASCENSIA DIABETES CARE US INC.
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