FDA UDI In Commercial Distribution 🇺🇸 United States

Dukal

DI: 10665973002818 · Model: 2495 · Dukal LLC
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
10

Basic Information

Brand Name
Dukal
Primary DI
10665973002818
Version / Model
2495
Catalog Number
2495
Company Name
Dukal LLC
Labeler DUNS
791014871
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
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
bd1c91f1-622b-4044-a95c-6b80b6c37f63

Device Description

Super Sponges Medium 32-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

Identifiers

Type ID
Package 20665973002815
Primary 10665973002818
Unit of Use 00665973002811

Customer Contacts

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