DermaView Transparent Dressing

GUDID 00714196151162

DERMARITE INDUSTRIES LLC

Synthetic polymer semi-permeable film dressing, adhesive, sterile Synthetic polymer semi-permeable film dressing, adhesive, sterile Synthetic polymer semi-permeable film dressing, adhesive, sterile Synthetic polymer semi-permeable film dressing, adhesive, sterile Synthetic polymer semi-permeable film dressing, adhesive, sterile Synthetic polymer semi-permeable film dressing, adhesive, sterile Synthetic polymer semi-permeable film dressing, adhesive, sterile Synthetic polymer semi-permeable film dressing, adhesive, sterile Synthetic polymer semi-permeable film dressing, adhesive, sterile Synthetic polymer semi-permeable film dressing, adhesive, sterile Synthetic polymer semi-permeable film dressing, adhesive, sterile Synthetic polymer semi-permeable film dressing, adhesive, sterile Synthetic polymer semi-permeable film dressing, adhesive, sterile Synthetic polymer semi-permeable film dressing, adhesive Synthetic polymer semi-permeable film dressing, adhesive Synthetic polymer semi-permeable film dressing, adhesive Synthetic polymer semi-permeable film dressing, adhesive Synthetic polymer semi-permeable film dressing, adhesive Synthetic polymer semi-permeable film dressing, adhesive Synthetic polymer semi-permeable film dressing, adhesive Synthetic polymer semi-permeable film dressing, adhesive Synthetic polymer semi-permeable film dressing, adhesive Synthetic polymer semi-permeable film dressing, adhesive Synthetic polymer semi-permeable film dressing, adhesive Synthetic polymer semi-permeable film dressing, adhesive Synthetic polymer semi-permeable film dressing, adhesive Synthetic polymer semi-permeable film dressing, adhesive
Primary Device ID00714196151162
NIH Device Record Keybb476626-43f6-4bfd-a0f0-d1acc6312ad9
Commercial Distribution StatusIn Commercial Distribution
Brand NameDermaView Transparent Dressing
Version Model Number15611
Company DUNS883925562
Company NameDERMARITE INDUSTRIES LLC
Device Count10
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100714196151162 [Primary]
GS101714196151161 [Unit of Use]

FDA Product Code

KMKDevice, Intravascular Catheter Securement

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-09-09
Device Publish Date2020-09-01

On-Brand Devices [DermaView Transparent Dressing]

0071419615116215611
0071419639236715611

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