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 2019-06-28 for SAPH AP223-01 MBORE NV W/0.2FLTR BCV&PAV 163830401 manufactured by Icu Medical Costa Rica Ltd..
Report Number | 9615050-2019-00210 |
MDR Report Key | 8745191 |
Report Source | COMPANY REPRESENTATIVE,HEALTH |
Date Received | 2019-06-28 |
Date of Report | 2019-06-11 |
Date of Event | 2019-06-01 |
Date Mfgr Received | 2019-08-13 |
Date Added to Maude | 2019-06-28 |
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 | EMILY ARNOULD, BSN, RN |
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 | SAPH AP223-01 MBORE NV W/0.2FLTR BCV&PAV |
Generic Name | ACCESSORIES, PUMP, INFUSION |
Product Code | MRZ |
Date Received | 2019-06-28 |
Returned To Mfg | 2019-06-17 |
Catalog Number | 163830401 |
Lot Number | UNKNOWN |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Age | DA |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | ICU MEDICAL COSTA RICA LTD. |
Manufacturer Address | ZONA FRANCA GLOBAL LA AURORA HEREDIA CS |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2019-06-28 |