Silflex

GUDID 05060031472950

Soft silicone wound contact layer 8 cm X 10 cm. A wound contact layer made from polyester mesh and coated with Silfix soft silicone. Silflex is designed to gently adhere to the skin surrounding a wound and not to the wound bed. This is an atraumatic dressing designed to minimise the pain and trauma associated with dressing change. The dressing’s large perforations allow for the passage of exudate and irrigation of wound.

BRIGHTWAKE LIMITED

Wound-nonadherent dressing, permeable, non-antimicrobial Wound-nonadherent dressing, permeable, non-antimicrobial Wound-nonadherent dressing, permeable, non-antimicrobial Wound-nonadherent dressing, permeable, non-antimicrobial Wound-nonadherent dressing, permeable, non-antimicrobial Wound-nonadherent dressing, permeable, non-antimicrobial Wound-nonadherent dressing, permeable, non-antimicrobial Wound-nonadherent dressing, permeable, non-antimicrobial Wound-nonadherent dressing, permeable, non-antimicrobial Wound-nonadherent dressing, permeable, non-antimicrobial Wound-nonadherent dressing, permeable, non-antimicrobial Wound-nonadherent dressing, permeable, non-antimicrobial Wound-nonadherent dressing, permeable, non-antimicrobial Wound-nonadherent dressing, permeable, non-antimicrobial Wound-nonadherent dressing, permeable, non-antimicrobial Wound-nonadherent dressing, permeable, non-antimicrobial Wound-nonadherent dressing, permeable, non-antimicrobial
Primary Device ID05060031472950
NIH Device Record Keyabf81ac2-f63f-4f29-bcdc-bb72421f2069
Commercial Distribution StatusIn Commercial Distribution
Brand NameSilflex
Version Model NumberCR3923
Company DUNS226502201
Company NameBRIGHTWAKE LIMITED
Device Count1
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 Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+441623751500
Emailinfo@advancis.co.uk
Phone+441623751500
Emailinfo@advancis.co.uk
Phone+441623751500
Emailinfo@advancis.co.uk
Phone+441623751500
Emailinfo@advancis.co.uk
Phone+441623751500
Emailinfo@advancis.co.uk
Phone+441623751500
Emailinfo@advancis.co.uk
Phone+441623751500
Emailinfo@advancis.co.uk
Phone+441623751500
Emailinfo@advancis.co.uk
Phone+441623751500
Emailinfo@advancis.co.uk
Phone+441623751500
Emailinfo@advancis.co.uk
Phone+441623751500
Emailinfo@advancis.co.uk
Phone+441623751500
Emailinfo@advancis.co.uk
Phone+441623751500
Emailinfo@advancis.co.uk
Phone+441623751500
Emailinfo@advancis.co.uk
Phone+441623751500
Emailinfo@advancis.co.uk
Phone+441623751500
Emailinfo@advancis.co.uk
Phone+441623751500
Emailinfo@advancis.co.uk

Device Dimensions

Length10 Centimeter
Width8 Centimeter
Length10 Centimeter
Width8 Centimeter
Length10 Centimeter
Width8 Centimeter
Length10 Centimeter
Width8 Centimeter
Length10 Centimeter
Width8 Centimeter
Length10 Centimeter
Width8 Centimeter
Length10 Centimeter
Width8 Centimeter
Length10 Centimeter
Width8 Centimeter
Length10 Centimeter
Width8 Centimeter
Length10 Centimeter
Width8 Centimeter
Length10 Centimeter
Width8 Centimeter
Length10 Centimeter
Width8 Centimeter
Length10 Centimeter
Width8 Centimeter
Length10 Centimeter
Width8 Centimeter
Length10 Centimeter
Width8 Centimeter
Length10 Centimeter
Width8 Centimeter
Length10 Centimeter
Width8 Centimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS105060031472943 [Primary]
GS105060031472950 [Package]
Contains: 05060031472943
Package: Retail [10 Units]
In Commercial Distribution
GS105060031472967 [Package]
Package: Shipper [30 Units]
In Commercial Distribution

FDA Product Code

NADDressing, Wound, Occlusive

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-08-04
Device Publish Date2023-07-27

On-Brand Devices [Silflex]

05060031473872Soft silicone wound contact layer 35 cm X 60 cm. A wound contact layer made from polyester mesh
05060031473032Soft silicone wound contact layer 20 cm X 30 cm. A wound contact layer made from polyester mesh
05060031472981Soft silicone wound contact layer 12 cm X 15 cm. A wound contact layer made from polyester mesh
05060031472950Soft silicone wound contact layer 8 cm X 10 cm. A wound contact layer made from polyester mesh a
05060031472912Soft silicone wound contact layer 5 cm X 7 cm. A wound contact layer made from polyester mesh an

Trademark Results [Silflex]

Mark Image

Registration | Serial
Company
Trademark
Application Date
SILFLEX
SILFLEX
87561932 not registered Dead/Abandoned
Lanexa International LLC
2017-08-09
SILFLEX
SILFLEX
87289509 5270306 Live/Registered
HBD/Thermoid, Inc.
2017-01-04
SILFLEX
SILFLEX
85552280 4311796 Live/Registered
Brightwake Limited
2012-02-24
SILFLEX
SILFLEX
79134661 4948388 Live/Registered
EIS Optics Limited
2013-03-19
SILFLEX
SILFLEX
79134633 not registered Dead/Abandoned
Friedrich Lütze GmbH
2013-06-03
SILFLEX
SILFLEX
77960953 4106110 Live/Registered
American Ceramic Technology
2010-03-17
SILFLEX
SILFLEX
76523525 2839933 Dead/Cancelled
Interton
2003-05-27
SILFLEX
SILFLEX
74509392 1923199 Live/Registered
BASF LEC CONSTRUCTION CHEMICALS, LLC
1994-04-01
SILFLEX
SILFLEX
74346893 1790098 Live/Registered
DENTSPLY SIRONA INC.
1993-01-11
SILFLEX
SILFLEX
73713308 1555383 Dead/Cancelled
CIBA-GEIGY CORPORATION
1988-02-25
SILFLEX
SILFLEX
73701475 1506735 Dead/Cancelled
LES ETABLISSEMENTS GIVAUDAN, LAVIROTTE ET CIE
1987-12-17
SILFLEX
SILFLEX
72407024 0975010 Dead/Cancelled
H. K. PORTER COMPANY, INC.
1971-11-05

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