FDA UDI In Commercial Distribution 🇺🇸 United States

Dukal

DI: 10665973003495 · Model: 8501 · 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
10665973003495
Version / Model
8501
Catalog Number
8501
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
cc1da2b1-d89c-4154-b521-38e8157a3fda

Device Description

Gauze Sponge, Basic Care, 3" x 3" 12-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 20665973003492
Primary 10665973003495
Package 30665973003499
Unit of Use 00665973003498

Customer Contacts

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