FDA Adverse Event Injury Summary report: N

LA8513 - HOOK SUCT COAGULATOR RIGHT ANGLED 33CM

MDR report key: 5015841 · Received July 27, 2015

Report

Report Number
1421101-2015-00001
Event Type
Injury
Date Received
July 27, 2015
Manufacturer
INSTRUMED INTERNATIONAL, INC.
Product Code
GEI
PMA / PMN Number
K040855
Report Source
Manufacturer report

Narratives

Description of Event or Problem · 1

(B)(4).

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
487585 LA8513 - HOOK SUCT COAGULATOR RIGHT ANGLED 33CM HOOK SUCT COAGULATOR RIGHT ANGLED GEI INSTRUMED INTERNATIONAL, INC.

Patients

Seq Age Sex Outcome Treatment
1