Brand Name | ZM-531PA |
Type of Device | TRANSMITTER |
Manufacturer (Section D) |
NIHON KOHDEN CORPORATION |
1-31-4 nishiochia, shinjuku-ku |
attn: shama mooman |
tokyo, japan 161-8 560 |
JA 161-8560 |
|
Manufacturer (Section G) |
NIHON KOHDEN CORPORATION |
1-31-4 nishiochia, shinjuku-ku |
attn: shama mooman |
gunma 161-8 560 |
JA
161-8560
|
|
Manufacturer Contact |
shama
mooman
|
safety mgmt dept, quality mgmt |
seibu bldg 2, 4th floor 1-11-2 |
kusunokidai tokorozawa, saitama 359-8-580
|
JA
359-8580
|
2687488
|
|
MDR Report Key | 5125860 |
MDR Text Key | 27644609 |
Report Number | 8030229-2015-00283 |
Device Sequence Number | 1 |
Product Code |
DRG
|
Combination Product (y/n) | N |
Reporter Country Code | US |
PMA/PMN Number | K043517 |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
user facility |
Reporter Occupation |
Other
|
Type of Report
| Followup |
Report Date |
10/02/2015,09/02/2015 |
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 |
Health Professional
|
Device Model Number | ZM-531PA |
Device Catalogue Number | ZM-531PA |
Was Device Available for Evaluation? |
Device Returned to Manufacturer
|
Date Returned to Manufacturer | 09/18/2015 |
Is the Reporter a Health Professional? |
No
|
Was the Report Sent to FDA? |
Yes
|
Date Report Sent to FDA | 10/02/2015 |
Distributor Facility Aware Date | 09/02/2015 |
Event Location |
Hospital
|
Date Report to Manufacturer | 10/02/2015 |
Initial Date Manufacturer Received |
Not provided
|
Initial Date FDA Received | 10/02/2015 |
Supplement Dates Manufacturer Received | Not provided
|
Supplement Dates FDA Received | 05/16/2017
|
Was Device Evaluated by Manufacturer? |
Yes
|
Is the Device Single Use? |
No
|
Is This a Reprocessed and Reused Single-Use Device? |
No
|
Type of Device Usage |
Reuse
|
Patient Sequence Number | 1 |
|
|