gudid
Primary ID: 7751
CONTOUR NEXT and MICROLET (UDI 7751)
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 and MICROLET - Primary ID 7751
Device Regulatory Overview
The CONTOUR NEXT and MICROLET (Model/Catalog Number: 7751) is a medical device manufactured by ASCENSIA DIABETES CARE US INC.. This product is indexed under FDA Product Code / Category Classification FMK within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 7751
- Product Code / EMDN
- FMK
- Device Name
- Mixed product shipper case containing 3 cartons of CONTOUR NEXT Blood Glucose Test Strips (Package DI Number 00301937312212) and 300 MICROLET colored lancets (provided sterile).
- Database Sync Date
- 2026-08-09 09:59:18
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 and MICROLET?
The registered manufacturer of record for CONTOUR NEXT and MICROLET is ASCENSIA DIABETES CARE US INC..
What is the Primary UDI-DI identifier for CONTOUR NEXT and MICROLET?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 7751.
What classification code is assigned to this device?
This device is registered under product classification code FMK.
Similar Classification Devices (FMK)
Other Devices by ASCENSIA DIABETES CARE US INC.
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