QIIClass II
Integrated Continuous Glucose Monitoring System For Professional Directed Retrospective Or Real-time Use
Clinical Chemistry · 21 CFR 862.1355
An integrated continuous glucose monitoring system for professional directed retrospective or real-time use is a continuous glucose recording device indicated for use as directed by a physician either for the real-time management of diabetes at home or for the retrospective discovery, analysis, and interpretation of glycemic variability in persons age 2 and older by healthcare professionals to guide appropriate patient management. The system is also intended to interface with digitally connected devices.
MDR events237All time
Recalls0All time
Registered firms8Currently listed
510(k) clearances1All time
Recent MDR events
237 adverse event reports on file
- DEXCOM G6 PROFESSIONAL SYSTEMMay 28, 2025MalfunctionDexcom, Inc.3004753838-2025-130486
- DEXCOM G6 PROFESSIONAL SYSTEMMay 15, 2025MalfunctionDexcom, Inc.3004753838-2025-119419
- DEXCOM G6 PROFESSIONAL SYSTEMMay 5, 2025MalfunctionDexcom, Inc.3004753838-2025-107465
- DEXCOM G6 PROFESSIONAL SYSTEMDec 16, 2024MalfunctionDexcom, Inc.3004753838-2024-330304
- DEXCOM G6 PROFESSIONAL SYSTEMDec 3, 2024MalfunctionDexcom, Inc.3004753838-2024-315601
- DEXCOM G6 PROFESSIONAL SYSTEMDec 3, 2024MalfunctionDexcom, Inc.3004753838-2024-316489
- DEXCOM G6 PROFESSIONAL SYSTEMDec 3, 2024MalfunctionDexcom, Inc.3004753838-2024-316501
- DEXCOM G6 PROFESSIONAL SYSTEMNov 24, 2024MalfunctionDexcom, Inc.3004753838-2024-309679
- DEXCOM G6 PROFESSIONAL SYSTEMNov 19, 2024MalfunctionDexcom, Inc.3004753838-2024-302204
- DEXCOM G6 PROFESSIONAL SYSTEMAug 21, 2024MalfunctionDexcom, Inc.3004753838-2024-209394
Event type breakdown
Malfunction234
Injury2
Death1
Most-reported manufacturers
Recalls
0 recall events for this product code
No recalls on file for this product code.
Registered firms
8 firms currently registered for this product code
510(k) clearances
1 clearances for this product code