FDA UDI In Commercial Distribution 🇺🇸 United States

Natus

DI: 00382830040532 · Model: 019-425900 · NATUS NEUROLOGY INCORPORATED
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Natus
Primary DI
00382830040532
Version / Model
019-425900
Company Name
NATUS NEUROLOGY INCORPORATED
Labeler DUNS
874257488
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-14
Public Version
3
Public Version Date
2018-06-11
Public Version Status
Update
Public Device Record Key
3afd3f60-436c-4eaf-bf81-eb2f56d401a2

Device Description

ELC/IND REUSE SNGL FIBR 25MM

Device Characteristics

Single Use
No
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
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
["Moist Heat or Steam Sterilization", "Ethylene Oxide"]

Product Codes

Code Name
IKT Electrode, Needle, Diagnostic Electromyograph

GMDN Terms

Code Name
11441 Electromyographic needle electrode, single-use

Identifiers

Type ID
Primary 00382830040532