FDA UDI In Commercial Distribution 🇺🇸 United States

Kendall

DI: 10884521516595 · Model: 33136RKT · Covidien LP
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Kendall
Primary DI
10884521516595
Version / Model
33136RKT
Company Name
Covidien LP
Labeler DUNS
058614483
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-12-11
Public Version
1
Public Version Date
2021-12-22
Public Version Status
New
Public Device Record Key
3cebd34c-207a-4436-a8e9-a49897dff1fe

Device Description

DL Disposable Lead Set

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
MR Unsafe
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
IKD CABLE, ELECTRODE

GMDN Terms

Code Name
35562 Electrocardiographic lead set, reusable

Identifiers

Type ID
Package 20884521516592
Primary 10884521516595
Package 30884521516599

Customer Contacts