FDA UDI In Commercial Distribution 🇺🇸 United States

ProSomnus EVO [PH] Sleep and Snore Device with Patient Monitoring

DI: 00850022853029 · Model: EVO [PH] with Patient Monitoring · PROSOMNUS SLEEP TECHNOLOGIES
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ProSomnus EVO [PH] Sleep and Snore Device with Patient Monitoring
Primary DI
00850022853029
Version / Model
EVO [PH] with Patient Monitoring
Company Name
PROSOMNUS SLEEP TECHNOLOGIES
Labeler DUNS
075438768
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-03-29
Public Version
1
Public Version Date
2024-04-08
Public Version Status
New
Public Device Record Key
646e0256-73d7-42f9-b3b4-f08d68bb2850

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
LRK Device, Anti-Snoring
LQZ Device, Jaw Repositioning

GMDN Terms

Code Name
47526 Mandible-repositioning sleep-disordered breathing orthosis

Identifiers

Type ID
Primary 00850022853029

Premarket Submissions

Submission Number Supplement Number
K221889 000