Brand Name | NXSTAGE SYSTEM ONE |
Type of Device | HIGH PERMEABILITY HEMODIALYSIS SYSTEM |
Manufacturer (Section D) |
NXSTAGE MEDICAL, INC. |
350 merrimack street |
lawrence MA 01843 |
|
Manufacturer (Section G) |
MEDIMEXICO S. DE R. L. DE C. V |
av. valle imperial no. 10523 |
parque industrial valle sur |
tijuana 22180 |
MX
22180
|
|
Manufacturer Contact |
paula
rogalski
|
nxstage medical, inc |
350 merrimack street |
lawrence, MA 01843
|
9784505276
|
|
MDR Report Key | 8173288 |
MDR Text Key | 130623792 |
Report Number | 3003464075-2018-00070 |
Device Sequence Number | 1 |
Product Code |
KDI
|
Combination Product (y/n) | Y |
Reporter Country Code | US |
PMA/PMN Number | K133547 |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
health professional |
Reporter Occupation |
Nurse
|
Type of Report
| Initial |
Report Date |
01/01/2005,12/18/2018 |
1 Device was Involved in the Event |
|
1 Patient was Involved in the Event |
|
Date FDA Received | 12/18/2018 |
Is this an Adverse Event Report? |
Yes
|
Is this a Product Problem Report? |
Yes
|
Device Operator |
Health Professional
|
Device Expiration Date | 05/01/2020 |
Device Model Number | CAR-505 |
Device Catalogue Number | CAR-505 |
Device Lot Number | 80878004 |
Was Device Available for Evaluation? |
No
|
Is the Reporter a Health Professional? |
Yes
|
Was the Report Sent to FDA? |
Yes
|
Date Report Sent to FDA | 01/01/2005 |
Date Report to Manufacturer | 01/10/2005 |
Date Manufacturer Received | 11/29/2018 |
Is This a Reprocessed and Reused Single-Use Device? |
No
|
Patient Sequence Number | 1 |
Patient Outcome(s) |
Required Intervention;
|
|
|