FDA UDI In Commercial Distribution 🇺🇸 United States

Dupress®

DI: 00809958092620 · Model: 9825 · Derma Sciences Canada Inc
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
40

Basic Information

Brand Name
Dupress®
Primary DI
00809958092620
Version / Model
9825
Catalog Number
DUP9825
Company Name
Derma Sciences Canada Inc
Labeler DUNS
200564891
Distribution Status
In Commercial Distribution
Device Count in Pkg
40
Record Status
Published
Publish Date
2018-10-23
Public Version
2
Public Version Date
2021-08-24
Public Version Status
Update
Public Device Record Key
e9cbf770-b2e9-4313-a88a-de660c6026ce

Device Description

9 in X 9 in, 8-ply Burn dressing. Bundled and packaged in 10s. 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
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 00809958092620
Unit of Use 00809958092606

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 9 in X 9 in
Device Size Text, specify 23 cm X 23 cm