FDA UDI In Commercial Distribution 🇺🇸 United States

Kendall

DI: 10885380206740 · Model: 33201B · Cardinal Health 200, LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
80

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Basic Information

Brand Name
Kendall
Primary DI
10885380206740
Version / Model
33201B
Catalog Number
33201B
Company Name
Cardinal Health 200, LLC
Labeler DUNS
961027315
Distribution Status
In Commercial Distribution
Device Count in Pkg
80
Record Status
Published
Publish Date
2025-06-10
Public Version
1
Public Version Date
2025-06-18
Public Version Status
New
Public Device Record Key
78d76f98-c944-4d14-8927-36fe4b60be13

Device Description

Kendall DL Multi B Code Single Patient Use System, 5 Lead ECG, SpO2, Temp, Bedside

Device Characteristics

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

Product Codes

Code Name
IKD CABLE, ELECTRODE

GMDN Terms

Code Name
31683 Electrocardiographic lead switching adaptor

Identifiers

Type ID
Unit of Use 20885380206747
Primary 10885380206740

Device Sizes

Type Value Unit Text
Length 10 Feet