DERMASOF DLP-1

GUDID 00852260000951

Areopexy, 2.75" OD x .75 ID x 5.90" L, 1 Pair

BIODERMIS CORPORATION

Scar management dressing, reusable
Primary Device ID00852260000951
NIH Device Record Key929e4461-4f0c-4ec5-861c-4d83714ef60e
Commercial Distribution StatusIn Commercial Distribution
Brand NameDERMASOF
Version Model NumberDLP-1
Catalog NumberDLP-1
Company DUNS809650005
Company NameBIODERMIS CORPORATION
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
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 Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Countertrue

Customer Support Contacts

Phone702-260-4466
Emailinfo@biodermis.com
Phone702-260-4466
Emailinfo@biodermis.com
Phone702-260-4466
Emailinfo@biodermis.com
Phone702-260-4466
Emailinfo@biodermis.com
Phone702-260-4466
Emailinfo@biodermis.com
Phone702-260-4466
Emailinfo@biodermis.com
Phone702-260-4466
Emailinfo@biodermis.com
Phone702-260-4466
Emailinfo@biodermis.com
Phone702-260-4466
Emailinfo@biodermis.com
Phone702-260-4466
Emailinfo@biodermis.com
Phone702-260-4466
Emailinfo@biodermis.com
Phone702-260-4466
Emailinfo@biodermis.com
Phone702-260-4466
Emailinfo@biodermis.com
Phone702-260-4466
Emailinfo@biodermis.com
Phone702-260-4466
Emailinfo@biodermis.com
Phone702-260-4466
Emailinfo@biodermis.com
Phone702-260-4466
Emailinfo@biodermis.com
Phone702-260-4466
Emailinfo@biodermis.com
Phone702-260-4466
Emailinfo@biodermis.com
Phone702-260-4466
Emailinfo@biodermis.com
Phone702-260-4466
Emailinfo@biodermis.com
Phone702-260-4466
Emailinfo@biodermis.com
Phone702-260-4466
Emailinfo@biodermis.com
Phone702-260-4466
Emailinfo@biodermis.com
Phone702-260-4466
Emailinfo@biodermis.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100852260000951 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

MDAElastomer, Silicone, For Scar Management

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-09-04
Device Publish Date2020-08-27

On-Brand Devices [DERMASOF]

00854763005501Mini Single sheet 5.7" x 2.5". 5 Sheets
00854763005495Square sheet 3" x 2.5". 5 Sheets
00854763005242Mini Single sheet 5.7" x 2.5". 1 Sheet
00854763005235Square sheet 3" x 2.5". 1 Sheet
00852260000968DermaSof Silicone Stick 4.25g tube.
00852260000951Areopexy, 2.75" OD x .75 ID x 5.90" L, 1 Pair
00852260000852Areola Circles 3" x .75", 1 Pair
00852260000845TNT Areola Circle 3" x .75", 1 Pair
00852260000838Mastopexy-L/R 12.6" x 3.8", 1 pair
00852260000821TNT Mastopexy-L/R 12.6" x 3.8". 1 Pair
00852260000814Strip 1.4" x 11.5". 1 Pair
00852260000807Large sheet 11" x 15.75". 1 Sheet
00852260000791Patch 2"x 2.5". 1 Pair
00852260000784Standard sheet 4.7" x 5.7". 1 Sheet
00852260000777Standard sheet 4.7" x 5.7". 5 Sheets
00852260000760TNT Strip 1.4" x 11.5". 1 Pair
00852260000753TNT Large sheet 11" x 15.75. 1 Sheet
00852260000746TNT Patch 2" x 2.5". 1 Pair
00852260000739Standard sheet 4.7" x 5.7". 1 Sheet
00852260000722TNT Standard sheet 4.7" x 5.7". 5 Sheets

Trademark Results [DERMASOF]

Mark Image

Registration | Serial
Company
Trademark
Application Date
DERMASOF
DERMASOF
98133536 not registered Live/Pending
Dermasof Inc.
2023-08-15
DERMASOF
DERMASOF
90235151 not registered Live/Pending
Biodermis Corporation
2020-10-05
DERMASOF
DERMASOF
76632997 3058626 Live/Registered
BIODERMIS CORPORATION
2005-03-07
DERMASOF
DERMASOF
75154203 2161328 Dead/Cancelled
INTELLECTUAL PROPERTY INT'L INC.
1996-08-22
DERMASOF
DERMASOF
74537225 not registered Dead/Abandoned
McGhan Medical Corporation
1994-06-13

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