FDA UDI In Commercial Distribution 🇺🇸 United States

Prosomnus IA MicrO2

DI: 00863039000423 · Model: MicrO2 · PROSOMNUS SLEEP TECHNOLOGIES
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Prosomnus IA MicrO2
Primary DI
00863039000423
Version / Model
MicrO2
Company Name
PROSOMNUS SLEEP TECHNOLOGIES
Labeler DUNS
075438768
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-06-21
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
dfa1105e-8d09-44cb-86aa-c3e21503c690

Device Description

Obstructive Sleep Apnea Device with twin mated posts

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
Yes
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

GMDN Terms

Code Name
47526 Mandible-repositioning sleep-disordered breathing orthosis

Identifiers

Type ID
Primary 00863039000423

Premarket Submissions

Submission Number Supplement Number
K133683 000