gudid
Primary ID: 7189
CONTOUR (UDI 7189)
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 - Primary ID 7189
Device Regulatory Overview
The CONTOUR (Model/Catalog Number: 7189) 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
- 7189
- Product Code / EMDN
- LFR
- Device Name
- Blood Glucose Monitoring System. For self-monitoring and management of blood glucose.Contents: CONTOUR Blood Glucose Meter; Quick Reference Guide; User Guide; Log Book; Carrying Case; Warranty Card.
- 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?
The registered manufacturer of record for CONTOUR is ASCENSIA DIABETES CARE US INC..
What is the Primary UDI-DI identifier for CONTOUR?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 7189.
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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