Aquasite® DUP81122

GUDID 00809958084410

Wound hydrogel dressing, sterile Wound hydrogel dressing, sterile

Primary Device ID	00809958084410
NIH Device Record Key	c82ac6a3-f529-4936-b329-6e100876a227
Commercial Distribution Status	In Commercial Distribution
Brand Name	Aquasite®
Version Model Number	81122
Catalog Number	DUP81122
Company DUNS	200564891
Company Name	Derma Sciences Canada Inc
Device Count	30
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 Issuing Agency	Device ID
GS1	00809958084403 [Unit of Use]
GS1	00809958084410 [Primary]

NAE	Dressing, wound, hydrogel without drug and/or biologic

Steralize Prior To Use	false
Device Is Sterile	true

00809958084410	2 in X 2 in Hydrogen impregnated non-woven dressing. Sterile.
00809958084212	4 in X 4 in Hydrogen impregnated non-woven dressing. Sterile.
00809958080016	Amorphous Hydrogel dressing. 1 oz. novel bellows tube.
00809958051818	2 in X 2 in Hydrogel impregnated guaze (woven). Sterile
00809958051719	4 in X 4 in Hydrogel impregnated guaze (woven). Sterile

Mark Image Registration \| Serial	Company Trademark Application Date
AQUASITE 74281757 1831860 Dead/Cancelled	InSite Vision Incorporated 1992-06-05