FDA UDI In Commercial Distribution 🇺🇸 United States

Dukal

DI: 10665973010127 · Model: 2085 · Dukal LLC
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
200

Basic Information

Brand Name
Dukal
Primary DI
10665973010127
Version / Model
2085
Catalog Number
2085
Company Name
Dukal LLC
Labeler DUNS
791014871
Distribution Status
In Commercial Distribution
Device Count in Pkg
200
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
1400b31f-56d1-4ae2-af03-40e4737817f6

Device Description

Gauze Pad 2" x 2" 8-Ply, 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
NAB Gauze / sponge,nonresorbable for external use

GMDN Terms

Code Name
48134 Woven gauze pad

Identifiers

Type ID
Package 20665973010124
Primary 10665973010127
Unit of Use 00665973010120

Customer Contacts

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