MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,health report with the FDA on 2020-03-30 for TRANSPAC? IT MONITORING KIT, 84" SAFESET RESERVOIR, 2 BLOOD SAMPLING PORT, 3ML F 42800-28 manufactured by Icu Medical De Mexico, S. De R.l. De C.v..
Report Number | 9617594-2020-00098 |
MDR Report Key | 9898148 |
Report Source | COMPANY REPRESENTATIVE,HEALTH |
Date Received | 2020-03-30 |
Date of Report | 2020-03-12 |
Date of Event | 2020-03-06 |
Date Mfgr Received | 2020-03-12 |
Device Manufacturer Date | 2019-06-01 |
Date Added to Maude | 2020-03-30 |
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 Contact | CHRISTOPHER ZANONI |
Manufacturer Street | 600 N. FIELD DR. |
Manufacturer City | LAKE FOREST IL 60045 |
Manufacturer Country | US |
Manufacturer Postal | 60045 |
Manufacturer Phone | 2247062300 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | TRANSPAC? IT MONITORING KIT, 84" SAFESET RESERVOIR, 2 BLOOD SAMPLING PORT, 3ML F |
Generic Name | TRANSDUCER, BLOOD-PRESSURE, EXTRAVASCULAR |
Product Code | DRS |
Date Received | 2020-03-30 |
Catalog Number | 42800-28 |
Lot Number | 4140090 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | ICU MEDICAL DE MEXICO, S. DE R.L. DE C.V. |
Manufacturer Address | AVENIDA CUARZO NO. 250 ENSENADA, B.CFA. 22790 MX 22790 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2020-03-30 |