FDA UDI In Commercial Distribution 🇺🇸 United States

DuCare®

DI: 00809958080214 · Model: 82212 · Derma Sciences Canada Inc
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
50

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Basic Information

Brand Name
DuCare®
Primary DI
00809958080214
Version / Model
82212
Catalog Number
DUP82212
Company Name
Derma Sciences Canada Inc
Labeler DUNS
200564891
Distribution Status
In Commercial Distribution
Device Count in Pkg
50
Record Status
Published
Publish Date
2018-10-23
Public Version
4
Public Version Date
2025-04-18
Public Version Status
Update
Public Device Record Key
ea3d23e7-97d8-4aca-99e7-3a9097f28567

Device Description

US-fold 2 in X 2 in 12 ply, 20 X 10 mesh gauze 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
48134 Woven gauze pad, non-antimicrobial

Identifiers

Type ID
Primary 00809958080214
Unit of Use 00809958080207

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