Advazorb Areola

GUDID 05060031479966

Absorbent foam dressing with soft silicone wound contact layer and border, 13cm x 13cm. A self adherent absorbent dressing with a Silfix® soft silicone wound contact layer and border. The dressing has an absorbent foam pad with high fluid handling capability. The soft silicone will adhere to surrounding dry skin but not to a wet wound. This is an atraumatic dressing which means it is designed to minimise the pain and trauma associated with dressing change. The film backing is breathable and prevents strike through.

BRIGHTWAKE LIMITED

Wound-nonadherent dressing, absorbent, non-antimicrobial Wound-nonadherent dressing, absorbent, non-antimicrobial Wound-nonadherent dressing, absorbent, non-antimicrobial Wound-nonadherent dressing, absorbent, non-antimicrobial Wound-nonadherent dressing, absorbent, non-antimicrobial Wound-nonadherent dressing, absorbent, non-antimicrobial Wound-nonadherent dressing, absorbent, non-antimicrobial Wound-nonadherent dressing, absorbent, non-antimicrobial Wound-nonadherent dressing, absorbent, non-antimicrobial Wound-nonadherent dressing, absorbent, non-antimicrobial Wound-nonadherent dressing, absorbent, non-antimicrobial Wound-nonadherent dressing, absorbent, non-antimicrobial Wound-nonadherent dressing, absorbent, non-antimicrobial Wound-nonadherent dressing, absorbent, non-antimicrobial Wound-nonadherent dressing, absorbent, non-antimicrobial Wound-nonadherent dressing, absorbent, non-antimicrobial Wound-nonadherent dressing, absorbent, non-antimicrobial
Primary Device ID05060031479966
NIH Device Record Key09bda766-9072-45fe-ab84-eda80b2279b5
Commercial Distribution StatusIn Commercial Distribution
Brand NameAdvazorb Areola
Version Model NumberCR4490
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

Width13 Centimeter
Length13 Centimeter
Width13 Centimeter
Length13 Centimeter
Width13 Centimeter
Length13 Centimeter
Width13 Centimeter
Length13 Centimeter
Width13 Centimeter
Length13 Centimeter
Width13 Centimeter
Length13 Centimeter
Width13 Centimeter
Length13 Centimeter
Width13 Centimeter
Length13 Centimeter
Width13 Centimeter
Length13 Centimeter
Width13 Centimeter
Length13 Centimeter
Width13 Centimeter
Length13 Centimeter
Width13 Centimeter
Length13 Centimeter
Width13 Centimeter
Length13 Centimeter
Width13 Centimeter
Length13 Centimeter
Width13 Centimeter
Length13 Centimeter
Width13 Centimeter
Length13 Centimeter
Width13 Centimeter
Length13 Centimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS105060031479959 [Primary]
GS105060031479966 [Package]
Contains: 05060031479959
Package: Retail [10 Units]
In Commercial Distribution
GS105060031479973 [Package]
Package: Shipper [15 Units]
In Commercial Distribution

FDA Product Code

NACDressing, Wound, Hydrophilic

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

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