MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional report with the FDA on 2019-06-20 for CAMERA HEAD AC - C-MOUNT 242401 manufactured by Medos International Sàrl.
Report Number | 1221934-2019-57385 |
MDR Report Key | 8719720 |
Report Source | HEALTH PROFESSIONAL |
Date Received | 2019-06-20 |
Date of Report | 2019-05-21 |
Date of Event | 2019-05-21 |
Date Mfgr Received | 2019-05-21 |
Date Added to Maude | 2019-06-20 |
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 | KARA DITTY-BOVARD |
Manufacturer Street | 325 PARAMOUNT DRIVE |
Manufacturer City | RAYNHAM MA 02767 |
Manufacturer Country | US |
Manufacturer Postal | 02767 |
Manufacturer Phone | 6103142063 |
Manufacturer G1 | BRIDGEWATER DISTRIBUTION |
Manufacturer Street | 50 SCOTLAND BOULEVARD |
Manufacturer City | BRIDGEWATER MA 02324 |
Manufacturer Country | US |
Manufacturer Postal Code | 02324 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | CAMERA HEAD AC - C-MOUNT |
Generic Name | ENDOSCOPIC VIDEO CAMERA |
Product Code | FWF |
Date Received | 2019-06-20 |
Catalog Number | 242401 |
Operator | HEALTH PROFESSIONAL |
Device Availability | Y |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | MEDOS INTERNATIONAL SàRL |
Manufacturer Address | CHEMIN-BLANC 38 LE LOCLE 02400 SZ 02400 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2019-06-20 |