FDA UDI In Commercial Distribution 🇺🇸 United States

Durlix®

DI: 00809958090411 · Model: 9344 · Derma Sciences Canada Inc
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Durlix®
Primary DI
00809958090411
Version / Model
9344
Catalog Number
DUP9344
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
2
Public Version Date
2020-11-19
Public Version Status
Update
Public Device Record Key
d59f5ea0-5ac7-42ed-a25e-78834bf5e0e4

Device Description

4 in X 4 in , 3-ply, "Krinkle" type sponge. Medium. Sterilized. Bulk

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
44971 General-purpose surgical sponge

Identifiers

Type ID
Primary 00809958090411

Customer Contacts

Device Sizes

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