FDA UDI In Commercial Distribution 🇺🇸 United States

Dukal

DI: 10665973020935 · Model: 11127 · Dukal LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Dukal
Primary DI
10665973020935
Version / Model
11127
Catalog Number
11127
Company Name
Dukal LLC
Labeler DUNS
791014871
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2026-01-30
Public Version
1
Public Version Date
2026-02-09
Public Version Status
New
Public Device Record Key
97f62b9f-bcac-4d62-afaf-2dad4b8f5266

Device Description

Gauze Fluffs Super Sponge 30"x36"

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
Yes
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 20665973020932
Primary 10665973020935

Customer Contacts

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