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

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
2
Public Version Date
2021-08-24
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

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