FDA UDI In Commercial Distribution 🇺🇸 United States

Dukal

DI: 00665973006901 · Model: C5119 · Dukal LLC
Product Codes
1
GMDN Terms
1
Identifiers
4
Pkg Device Count
2

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Basic Information

Brand Name
Dukal
Primary DI
00665973006901
Version / Model
C5119
Catalog Number
C5119
Company Name
Dukal LLC
Labeler DUNS
791014871
Distribution Status
In Commercial Distribution
Device Count in Pkg
2
Record Status
Published
Publish Date
2022-12-06
Public Version
2
Public Version Date
2025-04-18
Public Version Status
Update
Public Device Record Key
fd3b4a7c-1f0b-410e-8096-8fccfdedae0a

Device Description

Type VII Gauze Sponges 2" x 2" 8-Ply, 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
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 10665973006908
Primary 00665973006901
Package 20665973006905
Unit of Use 40665973006909

Customer Contacts

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