FDA UDI In Commercial Distribution 🇺🇸 United States

DuCare®

DI: 00809958030912 · Model: 3053 · Derma Sciences Canada Inc
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
DuCare®
Primary DI
00809958030912
Version / Model
3053
Catalog Number
DUP3053
Company Name
Derma Sciences Canada Inc
Labeler DUNS
200564891
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-10-23
Public Version
2
Public Version Date
2021-08-24
Public Version Status
Update
Public Device Record Key
b8deb6c5-cd12-48f3-9a32-79e739744cd1

Device Description

1.25 in Single Strugn Tonsil Sponge. X-Ray detectable

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
GDY GAUZE/SPONGE, INTERNAL, X-RAY DETECTABLE

GMDN Terms

Code Name
38496 Radiopaque woven surgical sponge

Identifiers

Type ID
Primary 00809958030912

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 1.25 in