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 2020-02-14 for INTUBATION PORTEX ENDOTRACHEAL TUBES SACETT 100/189/080 manufactured by Smiths Medical Asd,inc.
[179721282]
Information received a smith medical intubation
Patient Sequence No: 1, Text Type: D, B5
Report Number | 3012307300-2020-00807 |
MDR Report Key | 9714907 |
Report Source | COMPANY REPRESENTATIVE,HEALTH |
Date Received | 2020-02-14 |
Date of Report | 2020-02-14 |
Date of Event | 2020-01-01 |
Date Mfgr Received | 2020-01-15 |
Date Added to Maude | 2020-02-14 |
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 | DAVE HALVERSON |
Manufacturer Street | 6000 LANE N |
Manufacturer City | MINNEAPOLIS, MN |
Manufacturer Country | US |
Manufacturer Phone | 3833310 |
Manufacturer G1 | SMITHS MEDICAL ASD,INC. |
Manufacturer Street | 6000 NATHAN LANE NORTH |
Manufacturer City | MINNEAPOLIS, MN |
Manufacturer Country | US |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | INTUBATION PORTEX ENDOTRACHEAL TUBES SACETT |
Generic Name | TUBE, TRACHEAL/BRONCHIAL, DIFFERENTIAL VENTILATION (W/WO CONNECTOR) |
Product Code | CBI |
Date Received | 2020-02-14 |
Returned To Mfg | 2020-01-17 |
Model Number | INTUBATION PORTEX ENDOTRACHEAL TUBES SACETT |
Catalog Number | 100/189/080 |
Operator | HEALTH PROFESSIONAL |
Device Availability | R |
Device Eval'ed by Mfgr | N |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | SMITHS MEDICAL ASD,INC |
Manufacturer Address | 6000 LANE N MINNEAPOLIS, MN US |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2020-02-14 |