FDA UDI In Commercial Distribution 🇺🇸 United States

Aquasite®

DI: 00809958084410 · Model: 81122 · Derma Sciences Canada Inc
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
30

Basic Information

Brand Name
Aquasite®
Primary DI
00809958084410
Version / Model
81122
Catalog Number
DUP81122
Company Name
Derma Sciences Canada Inc
Labeler DUNS
200564891
Distribution Status
In Commercial Distribution
Device Count in Pkg
30
Record Status
Published
Publish Date
2018-10-23
Public Version
2
Public Version Date
2020-06-19
Public Version Status
Update
Public Device Record Key
c82ac6a3-f529-4936-b329-6e100876a227

Device Description

2 in X 2 in Hydrogen impregnated non-woven dressing. Sterile.

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

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

GMDN Terms

Code Name
47764 Wound hydrogel dressing, non-antimicrobial

Identifiers

Type ID
Primary 00809958084410
Unit of Use 00809958084403

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 2 in x 2 in
Device Size Text, specify 5 cm X 5 cm