FDA UDI In Commercial Distribution 🇺🇸 United States

Genio System 2.1

DI: 05404031024847 · Model: Genio Activation Chip Model #2364 · Nyxoah
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Genio System 2.1
Primary DI
05404031024847
Version / Model
Genio Activation Chip Model #2364
Catalog Number
NX-PKG-002484
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
42b18358-476f-42e7-b7a2-f350b81c1352

Device Description

The Activation Chip is the power source for the Implantable Stimulator. The Activation Chip contains a rechargeable battery, electronics for Bluetooth communication and electromagnetic power transmission, and a microprocessor that stores the user-specific stimulation parameters. The Activation Chip must be connected to the Disposable Patch and placed on the chin each night for stimulation to be delivered, and the battery must be recharged daily.

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
Yes
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 05404031024847

Premarket Submissions

Submission Number Supplement Number
P240024 000