FDA UDI In Commercial Distribution 🇺🇸 United States

NeoLead®

DI: 10812594011808 · Model: RadioLucent CE · Neotech Products LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
20

Basic Information

Brand Name
NeoLead®
Primary DI
10812594011808
Version / Model
RadioLucent CE
Catalog Number
N305CE
Company Name
Neotech Products LLC
Labeler DUNS
198013435
Distribution Status
In Commercial Distribution
Device Count in Pkg
20
Record Status
Published
Publish Date
2017-02-20
Public Version
6
Public Version Date
2023-09-20
Public Version Status
Update
Public Device Record Key
caf8948f-79c0-414e-bb74-6c815cdf5cf5

Device Description

NeoLead is a set of three/five ECG electrodes used on term neonates, infants, and pediatric patients. An electrocardiograph electrode (per FDA regulation# 870.2360 ) is the electrical conductor which is applied to the surface of the body to transmit the electrical signal at the body surface to a processor that produces an electrocardiogram or vectorcardiogram.

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
Yes
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
Yes
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
17460 Neonatal electrocardiographic electrode

Identifiers

Type ID
Primary 10812594011808
Unit of Use 00812594011801