FDA UDI In Commercial Distribution 🇺🇸 United States

DuSoft®

DI: 00809958091418 · Model: 94122 · Derma Sciences Canada Inc
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
DuSoft®
Primary DI
00809958091418
Version / Model
94122
Catalog Number
DUP94122
Company Name
Derma Sciences Canada Inc
Labeler DUNS
200564891
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-11-13
Public Version
3
Public Version Date
2021-09-24
Public Version Status
Update
Public Device Record Key
3cb4d131-719b-412a-a2f3-389dc9faeca0

Device Description

2 in X 2 in , 4-ply non-woven sponge. Non-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
No
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 00809958091418

Customer Contacts

Device Sizes

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