FDA UDI In Commercial Distribution 🇺🇸 United States

NIKOTRACE

DI: 10853512006902 · Model: 4039 · NIKOMED USA
Product Codes
1
GMDN Terms
1
Identifiers
4
Pkg Device Count
3

Basic Information

Brand Name
NIKOTRACE
Primary DI
10853512006902
Version / Model
4039
Catalog Number
4039
Company Name
NIKOMED USA
Labeler DUNS
073648341
Distribution Status
In Commercial Distribution
Device Count in Pkg
3
Record Status
Published
Publish Date
2025-03-21
Public Version
1
Public Version Date
2025-03-31
Public Version Status
New
Public Device Record Key
d528cff7-0228-4c30-b1d7-3de4956d6c73

Device Description

Repositionable ECG Electrodes

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 Conditional
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
DRX Electrode, electrocardiograph

GMDN Terms

Code Name
35035 Electrocardiographic electrode, single-use

Identifiers

Type ID
Package 20853512006909
Primary 10853512006902
Package 30853512006906
Unit of Use 00853512006905

Customer Contacts

Phone
+1(800)355-6456 ext. 205

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
41 – 86 Degrees Fahrenheit