FDA UDI In Commercial Distribution 🇺🇸 United States

Dukal

DI: 00665973017235 · Model: 262 · Dukal LLC
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Dukal
Primary DI
00665973017235
Version / Model
262
Catalog Number
262
Company Name
Dukal LLC
Labeler DUNS
791014871
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-12-06
Public Version
2
Public Version Date
2022-12-20
Public Version Status
Update
Public Device Record Key
e9c41805-59b1-42d7-9822-5f451f606af7

Device Description

Plain Packing Strip 1" x 5 yd

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
No
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
EFQ GAUZE/SPONGE, INTERNAL

GMDN Terms

Code Name
48128 Gauze strip, non-antimicrobial

Identifiers

Type ID
Package 10665973017232
Primary 00665973017235
Package 20665973017239

Customer Contacts

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

Premarket Submissions

Submission Number Supplement Number
K861154 000