FDA UDI In Commercial Distribution 🇺🇸 United States

PureSleep Pro

DI: 00851727004037 · Model: PSKITPROA · SLEEP SCIENCE PARTNERS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
PureSleep Pro
Primary DI
00851727004037
Version / Model
PSKITPROA
Catalog Number
PSKITPROA
Company Name
SLEEP SCIENCE PARTNERS, INC.
Labeler DUNS
808128693
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-07-30
Public Version
1
Public Version Date
2018-08-30
Public Version Status
New
Public Device Record Key
690c294e-531f-40c4-b8ea-7409f4c653f0

Device Description

One PureSleep PRO Anti-Snoring Device Kit US

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
No
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
LRK Device, Anti-Snoring

GMDN Terms

Code Name
47526 Mandible-repositioning sleep-disordered breathing orthosis

Identifiers

Type ID
Primary 00851727004037

Premarket Submissions

Submission Number Supplement Number
K113022 000