FDA UDI In Commercial Distribution 🇺🇸 United States

DuSoft®

DI: 00809958082416 · Model: 84918 · Derma Sciences Canada Inc
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
35

Basic Information

Brand Name
DuSoft®
Primary DI
00809958082416
Version / Model
84918
Catalog Number
DUP84918
Company Name
Derma Sciences Canada Inc
Labeler DUNS
200564891
Distribution Status
In Commercial Distribution
Device Count in Pkg
35
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
9d4abc2a-8871-4161-a83d-347df6c9d8b1

Device Description

2 in X 2 in non-woven, 6 ply drain sponge. 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 00809958082416
Unit of Use 00809958082409

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