L-CLIP APPL/REMVR 90 MM RND HANDLE VAR 45.441

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 99 report with the FDA on 2013-12-18 for L-CLIP APPL/REMVR 90 MM RND HANDLE VAR 45.441 manufactured by Peter Lazic Gmbh.

Event Text Entries

[21175919] Report received from the usa stating that "the applier will not close". No injury or medical intervention occurred. There was no additional info provided.
Patient Sequence No: 1, Text Type: D, B5


[21298249] The device was received by (b)(4). (b)(4) is the importer of the device. If additional info is received, a supplemental report will be sent. (b)(4).
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number1045834-2013-16094
MDR Report Key3981032
Report Source99
Date Received2013-12-18
Date of Report2012-06-18
Date of Event2012-06-15
Date Facility Aware2012-06-18
Report Date2012-06-18
Date Added to Maude2014-08-06
Event Key0
Report Source CodeDistributor report
Manufacturer LinkN
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer Street4500 RIVERSIDE DR.
Manufacturer CityPALM BEACH GARDENS FL 33410
Manufacturer CountryUS
Manufacturer Postal33410
Manufacturer G1THE ANSPACH EFFORT, INC.
Manufacturer Street4500 RIVERSIDE DR.
Manufacturer CityPALM BEACH GARDENS FL 33410
Manufacturer CountryUS
Manufacturer Postal Code33410
Single Use0
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameL-CLIP APPL/REMVR 90 MM RND HANDLE VAR
Generic NameNONE
Product CodeHCI
Date Received2013-12-18
Catalog Number45.441
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerPETER LAZIC GMBH
Manufacturer AddressTUTTLINGEN GM


Patients

Patient NumberTreatmentOutcomeDate
10 2013-12-18

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