FDA UDI Not in Commercial Distribution 🇺🇸 United States

Neuroline SubdermalNeurology Needle Electrodes

DI: 05707480121380 · Model: 74512-150/24G · Ambu A/S
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Neuroline SubdermalNeurology Needle Electrodes
Primary DI
05707480121380
Version / Model
74512-150/24G
Catalog Number
74512-150/24G
Company Name
Ambu A/S
Labeler DUNS
305682023
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-22
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
f72f55db-bdee-4a17-af24-8c7a8a12ca15
Distribution End Date
2018-03-09

Device Description

Ambu Neuroline Subdermal - Green wires only - USA

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
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
IKT Electrode, needle, diagnostic electromyograph

GMDN Terms

Code Name
47714 Subdermal needle electrode

Identifiers

Type ID
Package 05707480121403
Package 05707480121397
Primary 05707480121380

Customer Contacts

Phone
+14107686464

Device Sizes

Type Value Unit Text
Length 12 Millimeter
Length 150 Centimeter

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
10 – 40 Degrees Celsius