AquaRite Extra CMC 40220

GUDID 00714196390066

DERMARITE INDUSTRIES LLC

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 ID	00714196390066
NIH Device Record Key	93648969-cba5-4405-a291-95ffc91fd0cf
Commercial Distribution Status	In Commercial Distribution
Brand Name	AquaRite Extra CMC
Version Model Number	40220
Catalog Number	40220
Company DUNS	883925562
Company Name	DERMARITE INDUSTRIES LLC
Device Count	1
DM Exempt	false
Pre-market Exempt	true
MRI Safety Status	Labeling does not contain MRI Safety Information
Human Cell/Tissue Product	false
Device Kit	false
Device Combination Product	false
Single Use	true
Lot Batch	true
Serial Number	false
Manufacturing Date	false
Expiration Date	true
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	true
RX Perscription	false
OTC Over-The-Counter	false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00714196390066 [Primary]

FDA Product Code

NAC	Dressing, Wound, Hydrophilic

Sterilization

Steralize Prior To Use	false
Device Is Sterile	true

Device Entry Metadata

Public Version Status	New
Device Record Status	Published
Public Version Number	1
Public Version Date	2021-09-17
Device Publish Date	2021-09-09

On-Brand Devices [AquaRite Extra CMC]

00714196406606	40660
00714196404503	40450
00714196403186	40318
00714196402202	40220
00714196390127	40660
00714196390103	40450
00714196390080	40318
00714196390066	40220