Eclypse Contour

GUDID 05060031479683

Superabsorbent multisite dressing, 30cm X 51cm. Eclypse Contour is an exudate management wound dressing especially designed to fit to body contours. The dressing combines a rapid wicking layer, a CrystaLock layer, which is highly absorbent and locks away exudate, a sub-backing layer for even exudate distribution and a non-strikethrough backing to prevent leakage.

BRIGHTWAKE LIMITED

Exudate-absorbent dressing, hydrophilic-gel, non-antimicrobial Exudate-absorbent dressing, hydrophilic-gel, non-antimicrobial Exudate-absorbent dressing, hydrophilic-gel, non-antimicrobial Exudate-absorbent dressing, hydrophilic-gel, non-antimicrobial Exudate-absorbent dressing, hydrophilic-gel, non-antimicrobial Exudate-absorbent dressing, hydrophilic-gel, non-antimicrobial Exudate-absorbent dressing, hydrophilic-gel, non-antimicrobial Exudate-absorbent dressing, hydrophilic-gel, non-antimicrobial Exudate-absorbent dressing, hydrophilic-gel, non-antimicrobial Exudate-absorbent dressing, hydrophilic-gel, non-antimicrobial Exudate-absorbent dressing, hydrophilic-gel, non-antimicrobial Exudate-absorbent dressing, hydrophilic-gel, non-antimicrobial Exudate-absorbent dressing, hydrophilic-gel, non-antimicrobial Exudate-absorbent dressing, hydrophilic-gel, non-antimicrobial Exudate-absorbent dressing, hydrophilic-gel, non-antimicrobial Exudate-absorbent dressing, hydrophilic-gel, non-antimicrobial Exudate-absorbent dressing, hydrophilic-gel, non-antimicrobial
Primary Device ID05060031479683
NIH Device Record Keyfcf93735-aea7-4152-a3f8-daeddfdcb652
Commercial Distribution StatusIn Commercial Distribution
Brand NameEclypse Contour
Version Model NumberCR4398
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

Length51 Centimeter
Width30 Centimeter
Length51 Centimeter
Width30 Centimeter
Length51 Centimeter
Width30 Centimeter
Length51 Centimeter
Width30 Centimeter
Length51 Centimeter
Width30 Centimeter
Length51 Centimeter
Width30 Centimeter
Length51 Centimeter
Width30 Centimeter
Length51 Centimeter
Width30 Centimeter
Length51 Centimeter
Width30 Centimeter
Length51 Centimeter
Width30 Centimeter
Length51 Centimeter
Width30 Centimeter
Length51 Centimeter
Width30 Centimeter
Length51 Centimeter
Width30 Centimeter
Length51 Centimeter
Width30 Centimeter
Length51 Centimeter
Width30 Centimeter
Length51 Centimeter
Width30 Centimeter
Length51 Centimeter
Width30 Centimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS105060031479676 [Primary]
GS105060031479683 [Package]
Contains: 05060031479676
Package: Retail [10 Units]
In Commercial Distribution
GS105060031479690 [Package]
Package: Shipper [10 Units]
In Commercial Distribution

FDA Product Code

FQMBandage, Elastic

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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