FDA UDI In Commercial Distribution 🇺🇸 United States

Genio System 2.1

DI: 05404031000025 · Model: Genio Sleep Lab Application Software · Nyxoah
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Genio System 2.1
Primary DI
05404031000025
Version / Model
Genio Sleep Lab Application Software
Company Name
Nyxoah
Labeler DUNS
400460590
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-08-26
Public Version
1
Public Version Date
2025-09-03
Public Version Status
New
Public Device Record Key
ce6ef640-a974-4d24-aa30-e8aa444cc835

Device Description

The Genio Sleep Lab Application software is used to configure the Activation Chip stimulation parameters. This remote application runs on a small mini-computer (Repeater, provided as part of the Genio Sleep Lab Kit - Primary DI: 05404031025301) and uses Bluetooth low energy (BLE) protocol to enable the operator to configure/customize the Activation Chip stimulation parameters. Once the Activation Chip is connected to a Disposable Patch, the Sleep Lab Application can be used to perform Activation Chip check-ups, read usage data stored in the AC and program/adjust the stimulation parameters.

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

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
MNQ Stimulator, Hypoglossal Nerve, Implanted, Apnea

GMDN Terms

Code Name
60360 Implantable sleep apnoea treatment system, fixed-rate

Identifiers

Type ID
Primary 05404031000025

Premarket Submissions

Submission Number Supplement Number
P240024 000