gudid
Primary ID: 9767
CONTOUR NEXT ONE (UDI 9767)
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 ONE - Primary ID 9767
Device Regulatory Overview
The CONTOUR NEXT ONE (Model/Catalog Number: 9767) 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
- 9767
- Product Code / EMDN
- LFR
- Device Name
- Blood Glucose Monitoring System. 1 kit. For self-testing, monitoring and management of blood glucose.Kit contains: CONTOUR NEXT ONE blood glucose meter; 10 CONTOUR NEXT blood glucose test strips; Lancing Device; 10 Colored MICROLET lancets (provided sterile); User Guide (including CONTOUR DIABETES app download instructions); Quick Reference Guide; Carrying Case; Web Registration / Warranty Card; CONTOUR NEXT control solution. A clear endcap is available for Alternative Site Testing (AST). It may not be included in your meter kit. If you perform AST and need a clear endcap (for palm), contact Diabetes Care Customer Service.
- 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
}
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 CONTOUR NEXT ONE?
The registered manufacturer of record for CONTOUR NEXT ONE is ASCENSIA DIABETES CARE US INC..
What is the Primary UDI-DI identifier for CONTOUR NEXT ONE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 9767.
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.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint