MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional report with the FDA on 2020-03-29 for ATTAIN BIPOLAR OVER THE WIRE LEAD 419478 manufactured by Mpri.
[185519120]
Concomitant medical products: 694758 lead, implanted: (b)(6) 2007; w1tr01 crt-p, implanted: (b)(6) 2018. If information is provided in the future, a supplemental report will be issued.
Patient Sequence No: 1, Text Type: N, H10
[185519121]
It was reported that an interrogation showed an impedance warning on the left ventricular (lv) lead for low impedance. A high threshold reading was also noted on the right ventricular (rv) lead. Both leads remain in use. No patient complications have been reported as a result of this event.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 2649622-2020-06493 |
MDR Report Key | 9896104 |
Report Source | HEALTH PROFESSIONAL |
Date Received | 2020-03-29 |
Date of Report | 2020-03-29 |
Date of Event | 2020-03-06 |
Date Mfgr Received | 2020-03-11 |
Device Manufacturer Date | 2007-09-15 |
Date Added to Maude | 2020-03-29 |
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 | PAULA BIXBY |
Manufacturer Street | 8200 CORAL SEA ST NE |
Manufacturer City | MOUNDS VIEW MN 55112 |
Manufacturer Country | US |
Manufacturer Postal | 55112 |
Manufacturer Phone | 7635055378 |
Manufacturer G1 | MPRI |
Manufacturer Street | ROAD 149 KM 56.3 |
Manufacturer City | VILLALBA PR 00766 |
Manufacturer Country | US |
Manufacturer Postal Code | 00766 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | ATTAIN BIPOLAR OVER THE WIRE LEAD |
Generic Name | PULSE-GENERATOR, DUAL CHAMBER, IMPLANTABLE |
Product Code | LWP |
Date Received | 2020-03-29 |
Model Number | 419478 |
Catalog Number | 419478 |
Device Expiration Date | 2009-08-30 |
Operator | LAY USER/PATIENT |
Device Availability | N |
Device Eval'ed by Mfgr | * |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | MPRI |
Manufacturer Address | ROAD 149 KM 56.3 VILLALBA PR 00766 US 00766 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2020-03-29 |