FDA UDI Not in Commercial Distribution 🇺🇸 United States

Kendall

DI: 30884527017281 · Model: 4060 · Cardinal Health, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Kendall
Primary DI
30884527017281
Version / Model
4060
Catalog Number
4060
Company Name
Cardinal Health, Inc.
Labeler DUNS
080935429
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-24
Public Version
10
Public Version Date
2022-12-08
Public Version Status
Update
Public Device Record Key
10b69c83-34d0-4f73-86bf-0a49e1d62399
Distribution End Date
2021-02-18

Device Description

Ultrasound Gel Bottle

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
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
No
Sterilization Prior Use
No

Product Codes

Code Name
MUI Media,coupling,ultrasound

GMDN Terms

Code Name
15321 Skin topical coupling gel

Identifiers

Type ID
Package 20884527017284
Primary 30884527017281

Customer Contacts

Device Sizes

Type Value Unit Text
Total Volume 250 Milliliter

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
No;