FDA UDI In Commercial Distribution 🇺🇸 United States

Ducare®

DI: 00809958093320 · Model: 99212 · Derma Sciences Canada Inc
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
40

Basic Information

Brand Name
Ducare®
Primary DI
00809958093320
Version / Model
99212
Catalog Number
DUP99212
Company Name
Derma Sciences Canada Inc
Labeler DUNS
200564891
Distribution Status
In Commercial Distribution
Device Count in Pkg
40
Record Status
Published
Publish Date
2018-11-20
Public Version
3
Public Version Date
2023-04-04
Public Version Status
Update
Public Device Record Key
86442163-6b8f-443e-b16c-373717d790f0

Device Description

2 in X 2 in, H-Fold, 12-ply, 20 x 10 mesh Gauze sponges. 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
48127 Woven gauze roll/sheet

Identifiers

Type ID
Primary 00809958093320
Unit of Use 00809958093306

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 2 in x 2 in
Device Size Text, specify 5 cm x 5 cm