gudid
Primary ID: 7036
CONTOUR PLUS BLUE (UDI 7036)
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 PLUS BLUE - Primary ID 7036
Device Regulatory Overview
The CONTOUR PLUS BLUE (Model/Catalog Number: 7036) 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
- 7036
- Product Code / EMDN
- NBW
- Device Name
- "Contour Plus BlueBlood Glucose monitoring SystemFor Self- testing, mornitoring and management of blood glucose.Kit Contains:-Contour Plus Blue blood glucose meter (product of Indonesia)-Micolet Next Lancing device (Product of Poland) -User Guide-Quick Reference Guide- Carrying Case (Product of China)Control solutions are required but not included and must be purchased separately"
- 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 PLUS BLUE?
The registered manufacturer of record for CONTOUR PLUS BLUE is ASCENSIA DIABETES CARE US INC..
What is the Primary UDI-DI identifier for CONTOUR PLUS BLUE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 7036.
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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