MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a distributor,foreign report with the FDA on 2019-08-28 for SURGICAL TUBING 0037860 manufactured by Consolidated Medical Equipment.
Report Number | 3007305485-2019-00315 |
MDR Report Key | 8940145 |
Report Source | DISTRIBUTOR,FOREIGN |
Date Received | 2019-08-28 |
Date of Report | 2019-10-15 |
Date Mfgr Received | 2019-10-09 |
Device Manufacturer Date | 2018-09-18 |
Date Added to Maude | 2019-08-28 |
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 |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | MELANIE LANNON |
Manufacturer Street | 11311 CONCEPT BOULEVARD |
Manufacturer City | LARGO FL 33773 |
Manufacturer Country | US |
Manufacturer Postal | 33773 |
Manufacturer Phone | 7273995209 |
Manufacturer G1 | CONSOLIDATED MEDICAL EQUIPMENT |
Manufacturer Street | ALEJANDRO DUMAS AVE, 11321 COMPLEJO INDUSTRIAL CHIHUAHUA |
Manufacturer City | 31136 |
Manufacturer Country | MX |
Manufacturer Postal Code | 31136 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | SURGICAL TUBING |
Generic Name | SURGICAL TUBING |
Product Code | BYY |
Date Received | 2019-08-28 |
Returned To Mfg | 2019-09-04 |
Catalog Number | 0037860 |
Lot Number | 201809184 |
Device Availability | R |
Device Age | DA |
Device Eval'ed by Mfgr | Y |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | CONSOLIDATED MEDICAL EQUIPMENT |
Manufacturer Address | ALEJANDRO DUMAS AVE, 11321 COMPLEJO INDUSTRIAL CHIHUAHUA 31136 MX 31136 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2019-08-28 |