FDA UDI In Commercial Distribution 🇺🇸 United States

Dukal

DI: 10665973014095 · Model: 5340 · Dukal LLC
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
100

Basic Information

Brand Name
Dukal
Primary DI
10665973014095
Version / Model
5340
Catalog Number
5340
Company Name
Dukal LLC
Labeler DUNS
791014871
Distribution Status
In Commercial Distribution
Device Count in Pkg
100
Record Status
Published
Publish Date
2022-12-06
Public Version
1
Public Version Date
2022-12-14
Public Version Status
New
Public Device Record Key
106d4795-6a37-46a5-878a-b568420fc5af

Device Description

Top Sponges 4" x 4", Non-Sterile

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
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
NAC Dressing, wound, hydrophilic

GMDN Terms

Code Name
48134 Woven gauze pad

Identifiers

Type ID
Package 20665973014092
Primary 10665973014095
Unit of Use 00665973014098

Customer Contacts

Phone
+1(631)656-3800 ext. 172