MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,foreig report with the FDA on 2020-03-18 for PULSAR-18 T3 SEE MODEL NO. manufactured by Biotronik Ag, Buelach, Switzerland.
[183944795]
A pulsar-18 t3 stent system was chosen for treatment of a mildly calcified lesion in a mildly tortuous sfa. After successful deployment of the stent the device was removed from the patient's body. Upon removal it was detected that the inner shaft remained on the guide wire and was separated from the system. Lot number and size unavailable.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 1028232-2020-01322 |
MDR Report Key | 9849176 |
Report Source | COMPANY REPRESENTATIVE,FOREIG |
Date Received | 2020-03-18 |
Date of Report | 2020-03-13 |
Date of Event | 2019-12-18 |
Date Mfgr Received | 2020-03-13 |
Date Added to Maude | 2020-03-18 |
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 |
Reporter Occupation | OTHER HEALTH CARE PROFESSIONAL |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Street | 6024 JEAN ROAD |
Manufacturer City | LAKE OSWEGO OR 97035 |
Manufacturer Country | US |
Manufacturer Postal | 97035 |
Manufacturer Phone | 8772459800 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | PULSAR-18 T3 |
Generic Name | STENT, SUPERFICIAL FEMORAL ARTERY |
Product Code | NIP |
Date Received | 2020-03-18 |
Catalog Number | SEE MODEL NO. |
Operator | HEALTH PROFESSIONAL |
Device Availability | * |
Device Eval'ed by Mfgr | * |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | BIOTRONIK AG, BUELACH, SWITZERLAND |
Manufacturer Address | ACKERSTRASSE 6 BUELACH CH-8180 CH CH-8180 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2020-03-18 |