FDA UDI In Commercial Distribution 🇺🇸 United States

Dutex®

DI: 00809958070918 · Model: 76782 · Derma Sciences Canada Inc
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Dutex®
Primary DI
00809958070918
Version / Model
76782
Catalog Number
DUP76782
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
2023-04-04
Public Version Status
Update
Public Device Record Key
1c083b7e-86b1-4948-a899-bc663c12ef13

Device Description

3 in X 4.5 yards, 2 ply, 20X12 mesh gauze 100% cotton non-sterilized bandage roll.

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
48127 Woven gauze roll/sheet

Identifiers

Type ID
Primary 00809958070918

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 5 cm X 4.1 m
Device Size Text, specify 2 in X 4.5 yards