FDA UDI In Commercial Distribution 🇺🇸 United States

Dupress®

DI: 00809958084809 · Model: 8010 · Derma Sciences Canada Inc
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
Dupress®
Primary DI
00809958084809
Version / Model
8010
Catalog Number
DUP8010
Company Name
Derma Sciences Canada Inc
Labeler DUNS
200564891
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-10-23
Public Version
4
Public Version Date
2024-11-07
Public Version Status
Update
Public Device Record Key
ae2b3d89-1df1-4bb5-adcc-b5050afe5581

Device Description

25 in X 18 in folded into 7 in X 7 in - 16 ply, 20 X 24 mesh gauze burn dressing. Sterilized.

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
No
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
NAB Gauze / sponge,nonresorbable for external use

GMDN Terms

Code Name
48131 Non-woven gauze pad

Identifiers

Type ID
Primary 00809958084809

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 17.8 cm x 17.8 cm
Device Size Text, specify 7 in X 7 in