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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: ANGEL KISS LLC. UV PHOTOTHERAPY; LIGHT, ULTRAVIOLET, DERMATOLOGICAL

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ANGEL KISS LLC. UV PHOTOTHERAPY; LIGHT, ULTRAVIOLET, DERMATOLOGICAL Back to Search Results
Device Problem Adverse Event Without Identified Device or Use Problem (2993)
Patient Problems Radiation Burn (1755); Skin Irritation (2076)
Event Date 12/19/2020
Event Type  Injury  
Event Description
I bought this months ago and have been trying it with my psoriasis hoping it would be amazing, however it was not.It irritated my skin when using it and left the skin feeling more of a burn than before.It is dangerous that this lamp burns people like me.It is a rx medical device and should be removed from (b)(6).Here is the link of the lamp: (b)(6).Fda safety report id # (b)(4).
 
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Brand Name
UV PHOTOTHERAPY
Type of Device
LIGHT, ULTRAVIOLET, DERMATOLOGICAL
Manufacturer (Section D)
ANGEL KISS LLC.
MDR Report Key11273161
MDR Text Key230577854
Report NumberMW5099189
Device Sequence Number1
Product Code FTC
Combination Product (y/n)Y
Reporter Country CodeUS
Number of Events Reported1
Summary Report (Y/N)N
Report Source Voluntary
Reporter Occupation Patient
Type of Report Initial
Report Date 01/31/2021
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received02/02/2021
Is this an Adverse Event Report? Yes
Is this a Product Problem Report? Yes
Device Operator Lay User/Patient
Was Device Available for Evaluation? Yes
Patient Sequence Number1
Patient Outcome(s) Hospitalization; Life Threatening; Other; Required Intervention;
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