FDA UDI In Commercial Distribution 🇺🇸 United States

Kendall

DI: 10884527022052 · Model: MK00150 · Cardinal Health, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Kendall
Primary DI
10884527022052
Version / Model
MK00150
Catalog Number
MK00150
Company Name
Cardinal Health, Inc.
Labeler DUNS
080935429
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-24
Public Version
8
Public Version Date
2021-02-19
Public Version Status
Update
Public Device Record Key
c668eee6-f4bd-4a0e-b3e4-ac2e96ffa942

Device Description

3201L Apnea Products

Device Characteristics

Single Use
No
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
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
No
Sterilization Prior Use
No

Product Codes

Code Name
GXY ELECTRODE, CUTANEOUS

GMDN Terms

Code Name
35995 Transcutaneous electrical stimulation electrode, single-use

Identifiers

Type ID
Package 90884527022058
Primary 10884527022052

Customer Contacts

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
;