Brand Name | DEXCOM G5 MOBILE CONTINUOUS GLUCOSE MONITORING SYSTEM |
Type of Device | MDS |
Manufacturer (Section D) |
DEXCOM, INC. |
6340 sequence drive |
san diego CA 92121 |
|
Manufacturer (Section G) |
DEXCOM, INC. |
6340 sequence drive |
|
san diego CA 92121 |
|
Manufacturer Contact |
kipp
durbin
|
6340 sequence drive |
san diego, CA 92121
|
8582000200
|
|
MDR Report Key | 5439575 |
MDR Text Key | 38788923 |
Report Number | 3004753838-2016-05787 |
Device Sequence Number | 1 |
Product Code |
MDS
|
UDI-Device Identifier | 00386270000262 |
UDI-Public | (01)00386270000262(241)MT22719-PNK(10)5204957(17)NI |
Combination Product (y/n) | N |
Reporter Country Code | US |
PMA/PMN Number | P120005 |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
consumer |
Reporter Occupation |
Other
|
Type of Report
| Initial,Followup |
Report Date |
01/21/2016 |
1 Device was Involved in the Event |
|
1 Patient was Involved in the Event |
|
Is this an Adverse Event Report? |
No
|
Is this a Product Problem Report? |
Yes
|
Device Operator |
Lay User/Patient
|
Device Model Number | MT22719-PNK |
Device Catalogue Number | STR-GF-PNK |
Device Lot Number | 5204957 |
Was Device Available for Evaluation? |
Device Returned to Manufacturer
|
Date Returned to Manufacturer | 02/24/2016 |
Is the Reporter a Health Professional? |
No
|
Initial Date Manufacturer Received |
01/21/2016 |
Initial Date FDA Received | 02/16/2016 |
Supplement Dates Manufacturer Received | Not provided
|
Supplement Dates FDA Received | 04/03/2016
|
Was Device Evaluated by Manufacturer? |
Yes
|
Date Device Manufactured | 08/26/2015 |
Is the Device Single Use? |
No
|
Is This a Reprocessed and Reused Single-Use Device? |
No
|
Type of Device Usage |
Initial
|
Patient Sequence Number | 1 |
Patient Age | 24 YR |
Patient Weight | 61 |
|
|