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Adverse Event Report

ALIMED INC LEAD APRON   back to search results
Catalog Number 9-203
Event Description

Shielding products contain contaminated lead.

 
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Brand NameLEAD APRON
Type of DeviceLEAD APRON
Baseline Device 510(K) Number
Baseline Device PMA Number
Manufacturer (Section D)
ALIMED INC
297 high st
dedham MA 02026
Device Event Key104032
MDR Report Key105804
Event Key99468
Report NumberMW1011688
Device Sequence Number1
Product CodeEAJ
Report Source Voluntary
Report Date 07/15/1997
1 Device Was Involved in the Event
1 Patient Was Involved in the Event
Date FDA Received07/15/1997
Is This An Adverse Event Report? No
Is This A Product Problem Report? Yes
Device Operator Health Professional
Device Catalogue Number9-203
OTHER Device ID Number97-53580
Was Device Available For Evaluation? No Answer Provided
Is the Device an Implant? No
Is this an Explanted Device? No Answer Provided

Database last updated on February 28, 2009

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