FDA UDI In Commercial Distribution 🇺🇸 United States

DuCare®

DI: 00809958091111 · Model: 90412 · Derma Sciences Canada Inc
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
DuCare®
Primary DI
00809958091111
Version / Model
90412
Catalog Number
DUP90412
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
4
Public Version Date
2025-04-18
Public Version Status
Update
Public Device Record Key
19caed70-e869-4d8d-9e2e-e144ac32aba8

Device Description

4 in X 4 in, 12-ply, US-Fold 10 X 20 mesh gauze 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
48134 Woven gauze pad, non-antimicrobial

Identifiers

Type ID
Primary 00809958091111

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 10 cm X 10 cm
Device Size Text, specify 4 in X 4 in