MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional report with the FDA on 2019-08-26 for S8-3T MICRO TEE TRANSDUCER manufactured by Philips Ultrasound, Inc.
Report Number | 3019216-2019-00056 |
MDR Report Key | 8930559 |
Report Source | HEALTH PROFESSIONAL |
Date Received | 2019-08-26 |
Date of Report | 2019-08-01 |
Date Mfgr Received | 2019-08-01 |
Device Manufacturer Date | 2013-12-05 |
Date Added to Maude | 2019-08-26 |
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 | BIOMEDICAL ENGINEER |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | MR. PAUL CORRIGAN |
Manufacturer Street | 22100 BOTHELL EVERETT HIGHWAY |
Manufacturer City | BOTHELL WA 98021 |
Manufacturer Country | US |
Manufacturer Postal | 98021 |
Manufacturer Phone | 4254877000 |
Manufacturer G1 | PHILIPS MEDICAL SYSTEMS |
Manufacturer Street | 3000 MINUTEMAN ROAD |
Manufacturer City | ANDOVER MA 01810 |
Manufacturer Country | US |
Manufacturer Postal Code | 01810 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | S8-3T MICRO TEE TRANSDUCER |
Generic Name | S8-3T MICRO TEE TRANSDUCER |
Product Code | ITX |
Date Received | 2019-08-26 |
Lot Number | 03F9BL |
Operator | HEALTH PROFESSIONAL |
Device Availability | Y |
Device Age | DA |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | PHILIPS ULTRASOUND, INC |
Manufacturer Address | 22100 BOTHELL EVERETT HIGHWAY BOTHELL WA 98021 US 98021 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2019-08-26 |