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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: RANIR LLC GENTLE SLIDE FLOSSER

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RANIR LLC GENTLE SLIDE FLOSSER Back to Search Results
Device Problem Device Operates Differently Than Expected (2913)
Patient Problem Tooth Fracture (2428)
Event Date 03/13/2015
Event Type  Injury  
Event Description
Consumer claimed the flosser broke her tooth.
 
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Brand Name
GENTLE SLIDE FLOSSER
Type of Device
FLOSSER
Manufacturer (Section D)
RANIR LLC
4701 east paris se
grand rapids MI 49512 535
Manufacturer (Section G)
RANIR LLC
4701 east paris se
grand rapids MI 49512 535
Manufacturer Contact
elsa baker
4701 east paris ave se
grand rapids, MI 49512-5353
6166988880
MDR Report Key4682345
MDR Text Key5637464
Report Number1825660-2015-00014
Device Sequence Number1
Product Code JES
Combination Product (y/n)N
Reporter Country CodeUS
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type Consumer
Reporter Occupation Device Unattended
Type of Report Initial
Report Date 04/10/2015
1 Device was Involved in the Event
1 Patient was Involved in the Event
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Device Operator Other
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? No
Initial Date Manufacturer Received 03/13/2015
Initial Date FDA Received04/10/2015
Was Device Evaluated by Manufacturer? No
Is This a Reprocessed and Reused Single-Use Device? No
Type of Device Usage Initial
Patient Sequence Number1
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