FDA UDI In Commercial Distribution 🇺🇸 United States

Dukal

DI: 10665973015405 · Model: 402 · Dukal LLC
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
12

Basic Information

Brand Name
Dukal
Primary DI
10665973015405
Version / Model
402
Catalog Number
402
Company Name
Dukal LLC
Labeler DUNS
791014871
Distribution Status
In Commercial Distribution
Device Count in Pkg
12
Record Status
Published
Publish Date
2022-12-06
Public Version
2
Public Version Date
2023-04-04
Public Version Status
Update
Public Device Record Key
f0fc3baa-e74a-47fa-86d1-70b368a53e25

Device Description

Rolled Gauze 2" x 5 yd 2-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
48127 Woven gauze roll/sheet

Identifiers

Type ID
Package 20665973015402
Primary 10665973015405
Unit of Use 00665973015408

Customer Contacts

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