FDA UDI In Commercial Distribution 🇺🇸 United States

OtoNova Pro Clinical+TE+AABR

DI: 05060396173172 · Model: NPRO-CLN-DTA · OTODYNAMICS LIMITED
Product Codes
2
GMDN Terms
2
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
OtoNova Pro Clinical+TE+AABR
Primary DI
05060396173172
Version / Model
NPRO-CLN-DTA
Company Name
OTODYNAMICS LIMITED
Labeler DUNS
235908050
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-08-20
Public Version
1
Public Version Date
2024-08-28
Public Version Status
New
Public Device Record Key
72df1f79-0d34-4bbd-a580-458555ac78a8

Device Description

OtoNova Pro system for Clinical OAE and ABR hearing test applications. Includes OtoNova Pro instrument, ear probe, system items, and Clinical licence for the Nova-link app

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
EWO Audiometer
GWJ Stimulator, Auditory, Evoked Response

GMDN Terms

Code Name
35747 Evoked-potential audiometer
58019 Otoacoustic emission system, battery-powered

Identifiers

Type ID
Primary 05060396173172

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K234095 000