MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a distributor,foreign,other report with the FDA on 2019-09-20 for INTRODUCER KIT FOR GASTROSTOMY FEEDING TUBE, 18FR DILATOR 98431 109843103 manufactured by Avanos Medical Inc..
Report Number | 9611594-2019-00179 |
MDR Report Key | 9098088 |
Report Source | DISTRIBUTOR,FOREIGN,OTHER |
Date Received | 2019-09-20 |
Date of Report | 2019-09-20 |
Date Mfgr Received | 2019-09-06 |
Device Manufacturer Date | 2017-09-29 |
Date Added to Maude | 2019-09-20 |
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 |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | MS. LISA CLARK |
Manufacturer Street | 5405 WINDWARD PARKWAY |
Manufacturer City | ALPHARETTA GA 30004 |
Manufacturer Country | US |
Manufacturer Postal | 30004 |
Manufacturer Phone | 4704485444 |
Manufacturer G1 | AVENT SA DE R.L. DE C.V. (AVENT 1) |
Manufacturer Street | CIRCUITO INDUSTIAL NO.40 COLONIA OBRERA |
Manufacturer City | NOGALES, CP 84048 |
Manufacturer Country | MX |
Manufacturer Postal Code | 84048 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | INTRODUCER KIT FOR GASTROSTOMY FEEDING TUBE, 18FR DILATOR |
Generic Name | DH EF PERC PLACEMENT PRODUCTS |
Product Code | KGC |
Date Received | 2019-09-20 |
Model Number | 98431 |
Catalog Number | 109843103 |
Lot Number | AA7268R04 |
Device Expiration Date | 2019-08-01 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | AVANOS MEDICAL INC. |
Manufacturer Address | 5405 WINDWARD PARKWAY ALPHARETTA GA 30004 US 30004 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2019-09-20 |