MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,health professional report with the FDA on 2019-08-12 for LIFESTREAM BALLOON EXPANDABLE VASCULAR COVERED STENT LSM0800858 manufactured by Clearstream Technologies Ltd..
Report Number | 9616666-2019-00090 |
MDR Report Key | 8884045 |
Report Source | FOREIGN,HEALTH PROFESSIONAL |
Date Received | 2019-08-12 |
Date of Report | 2019-09-06 |
Date of Event | 2019-07-08 |
Date Mfgr Received | 2019-08-27 |
Device Manufacturer Date | 2019-01-02 |
Date Added to Maude | 2019-08-12 |
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 | PHARMACIST |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | JUDITH LUDWIG |
Manufacturer Street | 1415 W. 3RD STREET |
Manufacturer City | TEMPE AZ 85281 |
Manufacturer Country | US |
Manufacturer Postal | 85281 |
Manufacturer Phone | 4803032689 |
Manufacturer G1 | CLEARSTREAM TECHNOLOGIES LTD. |
Manufacturer Street | MOYNE UPPER |
Manufacturer City | ENNISCORTHY, CO. WEXFORD N A |
Manufacturer Country | EI |
Manufacturer Postal Code | N A |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | LIFESTREAM BALLOON EXPANDABLE VASCULAR COVERED STENT |
Generic Name | BALLOON EXPANDABLE VASCULAR COVERED STENT |
Product Code | PRL |
Date Received | 2019-08-12 |
Returned To Mfg | 2019-08-07 |
Catalog Number | LSM0800858 |
Lot Number | CMDN0012 |
Operator | HEALTH PROFESSIONAL |
Device Availability | R |
Device Age | DA |
Device Eval'ed by Mfgr | Y |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | CLEARSTREAM TECHNOLOGIES LTD. |
Manufacturer Address | MOYNE UPPER ENNISCORTHY, CO. WEXFORD N A EI N A |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2019-08-12 |