FDA UDI In Commercial Distribution 🇺🇸 United States

Kendall

DI: 00884521152178 · Model: MKN42634 · Cardinal Health, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Kendall
Primary DI
00884521152178
Version / Model
MKN42634
Catalog Number
MKN42634
Company Name
Cardinal Health, Inc.
Labeler DUNS
080935429
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-06-27
Public Version
3
Public Version Date
2020-08-07
Public Version Status
Update
Public Device Record Key
42e17440-79f1-4508-8f49-3e8e74642d26

Device Description

Alcohol Prep

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
No
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
LKB Pad, alcohol, device disinfectant

GMDN Terms

Code Name
61695 Skin-cleaning wipe, sterile

Identifiers

Type ID
Package 00884521195939
Primary 00884521152178
Package 00884521152161

Customer Contacts

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
;