FDA UDI In Commercial Distribution 🇺🇸 United States

Dukal

DI: 00665973010182 · Model: 879 · Dukal LLC
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Dukal
Primary DI
00665973010182
Version / Model
879
Catalog Number
879
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
1
Public Version Date
2022-12-14
Public Version Status
New
Public Device Record Key
32d1a1c9-f291-4b14-8e04-81dcc49edbb3

Device Description

DK Lube Jelly 2oz tube, ST

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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
KMJ Lubricant, patient

GMDN Terms

Code Name
60796 General-body orifice lubricant

Identifiers

Type ID
Package 10665973010189
Primary 00665973010182
Package 20665973010186

Customer Contacts

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