MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional,study report with the FDA on 2019-10-25 for ARISTA AH ABSORBABLE HEMOSTAT UNKAA097 manufactured by Davol Inc., Sub. C.r. Bard, Inc..
Report Number | 1213643-2019-10240 |
MDR Report Key | 9238492 |
Report Source | HEALTH PROFESSIONAL,STUDY |
Date Received | 2019-10-25 |
Date of Report | 2019-10-25 |
Date Mfgr Received | 2019-10-04 |
Date Added to Maude | 2019-10-25 |
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 | ANNA SMITH |
Manufacturer Street | 100 CROSSINGS BLVD. |
Manufacturer City | WARWICK RI 02886 |
Manufacturer Country | US |
Manufacturer Postal | 02886 |
Manufacturer Phone | 4018258449 |
Manufacturer G1 | MEDCHEM PRODUCTS, INC. -1223089 |
Manufacturer Street | 160 NEW BOSTON STREET |
Manufacturer City | WOBURN MA 01801 |
Manufacturer Country | US |
Manufacturer Postal Code | 01801 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | ARISTA AH ABSORBABLE HEMOSTAT |
Generic Name | AGENT, ABSORBABLE HEMOSTATIC, NON COLLAGEN BASED |
Product Code | LMG |
Date Received | 2019-10-25 |
Model Number | NA |
Catalog Number | UNKAA097 |
Lot Number | NI |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | DAVOL INC., SUB. C.R. BARD, INC. |
Manufacturer Address | 100 CROSSINGS BLVD. WARWICK RI 02886 US 02886 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Required No Informationntervention | 2019-10-25 |