Brand Name | SNOREGUARD |
Type of Device | DEVICE, ANTI-SNORING |
Manufacturer (Section D) |
RANIR LLC |
4701 east paris ave. se |
grand rapids MI 49512 5353 |
|
Manufacturer (Section G) |
RANIR LLC |
4701 east paris ave. se |
|
grand rapids MI 49512 5353 |
|
Manufacturer Contact |
rebekah
stenske
|
4701 east paris ave. se |
grand rapids, MI 49512-5353
|
6166988880
|
|
MDR Report Key | 6939705 |
MDR Text Key | 89617458 |
Report Number | 1825660-2017-00176 |
Device Sequence Number | 1 |
Product Code |
LRK
|
Combination Product (y/n) | N |
Reporter Country Code | CA |
PMA/PMN Number | K103004 |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
consumer |
Reporter Occupation |
Patient
|
Type of Report
| Initial |
Report Date |
10/11/2017 |
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 | SNORE GUARD BRAND |
Was Device Available for Evaluation? |
No
|
Is the Reporter a Health Professional? |
No
|
Distributor Facility Aware Date | 09/14/2017 |
Initial Date Manufacturer Received |
09/14/2017 |
Initial Date FDA Received | 10/11/2017 |
Is the Device Single Use? |
No
|
Is This a Reprocessed and Reused Single-Use Device? |
No
|
Type of Device Usage |
Unknown
|
Patient Sequence Number | 1 |
|
|