FDA UDI In Commercial Distribution 🇺🇸 United States

Medline

DI: 30080196291575 · Model: MDS032280 · MEDLINE INDUSTRIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
150

Basic Information

Brand Name
Medline
Primary DI
30080196291575
Version / Model
MDS032280
Catalog Number
MDS032280
Company Name
MEDLINE INDUSTRIES, INC.
Labeler DUNS
025460908
Distribution Status
In Commercial Distribution
Device Count in Pkg
150
Record Status
Published
Publish Date
2023-02-04
Public Version
1
Public Version Date
2023-02-13
Public Version Status
New
Public Device Record Key
30c1b2bc-5045-48fb-87f7-a54fd4a62a3b

Device Description

JELLY, LUBE, STERILE, FOIL PACK, 5G

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
No
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
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 40080196291572
Primary 30080196291575
Unit of Use 10080196291571

Customer Contacts