MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a consumer report with the FDA on 2018-02-09 for DEXCOM G5 MOBILE CONTINUOUS GLUCOSE MONITORING SYSTEM N/A SW10611 manufactured by Dexcom, Inc..
[99934780]
(b)(4).
Patient Sequence No: 1, Text Type: N, H10
[99934781]
Pt reported signal loss on (b)(6).
Patient Sequence No: 1, Text Type: D, B5
[104060022]
(b)(4).
Patient Sequence No: 1, Text Type: N, H10
[104060023]
Dexcom was made aware on (b)(4) 2018 that on (b)(6) 2018, a loss of connection between the transmitter and smart device occurred
Patient Sequence No: 1, Text Type: D, B5
Report Number | 3004753838-2018-014821 |
MDR Report Key | 7261852 |
Report Source | CONSUMER |
Date Received | 2018-02-09 |
Date of Report | 2018-02-09 |
Date of Event | 2018-01-13 |
Date Mfgr Received | 2018-02-09 |
Date Added to Maude | 2018-02-09 |
Event Key | 0 |
Report Source Code | Manufacturer report |
Manufacturer Link | Y |
Number of Patients in Event | 0 |
Adverse Event Flag | 3 |
Product Problem Flag | 3 |
Reprocessed and Reused Flag | 3 |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | MR KIPP DURBIN |
Manufacturer Street | 6340 SEQUENCE DR. |
Manufacturer City | SAN DIEGO CA 92121 |
Manufacturer Country | US |
Manufacturer Postal | 92121 |
Manufacturer Phone | 8582000200 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | DEXCOM G5 MOBILE CONTINUOUS GLUCOSE MONITORING SYSTEM |
Generic Name | CONTINUOUS GLUCOSE MONITOR |
Product Code | PQM |
Date Received | 2018-02-09 |
Model Number | N/A |
Catalog Number | SW10611 |
Operator | LAY USER/PATIENT |
Device Availability | N |
Device Age | DA |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | DEXCOM, INC. |
Manufacturer Address | 6340 SEQUENCE DR. SAN DIEGO CA 92121 US 92121 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2018-02-09 |