FDA UDI In Commercial Distribution 🇺🇸 United States

Kendall

DI: 10885380198007 · Model: 33204 · Cardinal Health 200, LLC
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

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Basic Information

Brand Name
Kendall
Primary DI
10885380198007
Version / Model
33204
Catalog Number
33204
Company Name
Cardinal Health 200, LLC
Labeler DUNS
961027315
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-03-06
Public Version
1
Public Version Date
2025-03-14
Public Version Status
New
Public Device Record Key
bf379b4b-5045-4d5f-96b4-639f82f7daf3

Device Description

Kendall DL Multi OEM Single Patient Use System, 5 Lead ECG, SpO2, Temp, Dual Connect Leadset Only

Device Characteristics

Single Use
Yes
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
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
Package 50885380198005
Package 20885380198004
Primary 10885380198007

Device Sizes

Type Value Unit Text
Length 3 Feet