FDA UDI In Commercial Distribution 🇺🇸 United States

Dukal

DI: 20665973032591 · Model: K-10040 · Dukal LLC
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
100

Basic Information

Brand Name
Dukal
Primary DI
20665973032591
Version / Model
K-10040
Catalog Number
K-10040
Company Name
Dukal LLC
Labeler DUNS
791014871
Distribution Status
In Commercial Distribution
Device Count in Pkg
100
Record Status
Published
Publish Date
2025-09-18
Public Version
1
Public Version Date
2025-09-26
Public Version Status
New
Public Device Record Key
2438b076-d6d1-4640-bbbc-49985b302202

Device Description

Pretreat Gauze 4x4, 12ply, Green

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
NAB Gauze / sponge,nonresorbable for external use

GMDN Terms

Code Name
48134 Woven gauze pad, non-antimicrobial

Identifiers

Type ID
Package 30665973032598
Primary 20665973032591
Unit of Use 00665973032597

Customer Contacts

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