FDA UDI In Commercial Distribution 🇺🇸 United States

Dupress®

DI: 00809958085134 · Model: 8136S · Derma Sciences Canada Inc
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Dupress®
Primary DI
00809958085134
Version / Model
8136S
Catalog Number
DUP8136S
Company Name
Derma Sciences Canada Inc
Labeler DUNS
200564891
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-03-08
Public Version
2
Public Version Date
2021-08-24
Public Version Status
Update
Public Device Record Key
ea790548-e7ca-49e1-a70b-4acd01c1e042

Device Description

18 in X 72 in 2 ply burn dressing folded into 3 in X 8 in - 96 ply. 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
Package 00809958085127
Primary 00809958085134

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 45.7 cm X 1.82 m
Device Size Text, specify 18 in X 72 in