FDA UDI In Commercial Distribution 🇺🇸 United States

Neuroline 720Neurology Surface Electrodes

DI: 05707480029112 · Model: 72001-K/12 · Ambu A/S
Product Codes
1
GMDN Terms
1
Identifiers
4
Pkg Device Count
12

Basic Information

Brand Name
Neuroline 720Neurology Surface Electrodes
Primary DI
05707480029112
Version / Model
72001-K/12
Catalog Number
72001-K/12
Company Name
Ambu A/S
Labeler DUNS
305682023
Distribution Status
In Commercial Distribution
Device Count in Pkg
12
Record Status
Published
Publish Date
2016-09-21
Public Version
3
Public Version Date
2023-12-18
Public Version Status
Update
Public Device Record Key
fa52080e-4188-4150-9b07-f18078f3d39a

Device Description

Wet Gel Electrodes K Connector Lead Wire Length: 10 cm (4")

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
No
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
GXY ELECTRODE, CUTANEOUS

GMDN Terms

Code Name
61020 Analytical non-scalp cutaneous electrode

Identifiers

Type ID
Package 05707480000678
Package 05707480029105
Primary 05707480029112
Unit of Use 05707480029129

Customer Contacts

Phone
+14107686464

Device Sizes

Type Value Unit Text
Length 10 Centimeter

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
10 – 25 Degrees Celsius