MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a user facility report with the FDA on 2019-11-25 for SMITHS MEDICAL BCI CAPNOGRAPHY MONITOR CAPNOCHECK II - 8400 8401 manufactured by Smiths Medical Asd, Inc..
Report Number | 3012307300-2019-06792 |
MDR Report Key | 9371229 |
Report Source | USER FACILITY |
Date Received | 2019-11-25 |
Date of Report | 2019-11-25 |
Date Mfgr Received | 2019-11-12 |
Device Manufacturer Date | 2012-02-03 |
Date Added to Maude | 2019-11-25 |
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 |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | DAVE HALVERSON |
Manufacturer Street | 6000 NATHAN LANE N |
Manufacturer City | MINNEAPOLIS MN 55442 |
Manufacturer Country | US |
Manufacturer Postal | 55442 |
Manufacturer G1 | SMITHS MEDICAL ASD, INC. |
Manufacturer Street | 3350 GRANADA AVENUE NORTH SUITE 100 |
Manufacturer City | OAKDALE MN 55128 |
Manufacturer Country | US |
Manufacturer Postal Code | 55128 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | SMITHS MEDICAL BCI CAPNOGRAPHY MONITOR CAPNOCHECK II - 8400 |
Generic Name | ANALYZER, GAS, CARBON-DIOXIDE, GASEOUS-PHASE |
Product Code | CCK |
Date Received | 2019-11-25 |
Returned To Mfg | 2019-08-06 |
Catalog Number | 8401 |
Device Availability | R |
Device Eval'ed by Mfgr | Y |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | SMITHS MEDICAL ASD, INC. |
Manufacturer Address | 6000 NATHAN LANE N MINNEAPOLIS MN 55442 US 55442 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2019-11-25 |