FDA UDI In Commercial Distribution 🇺🇸 United States

Provent Sleep Therapy

DI: 00868020000208 · Model: CAT1105 · PROVENT SLEEP THERAPY, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Provent Sleep Therapy
Primary DI
00868020000208
Version / Model
CAT1105
Catalog Number
CAT1105
Company Name
PROVENT SLEEP THERAPY, LLC
Labeler DUNS
080469780
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-08-25
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
1174e15c-8b26-47db-b8e8-465bb831697a

Device Description

Provent 30 Night Standard Pack contains 30 Standard resistance Provent

Device Characteristics

Single Use
Yes
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
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
OHP Expiratory Resistance Valve, Intranasal, For Obstructive Sleep Apnea

GMDN Terms

Code Name
11260 Nasal dilator

Identifiers

Type ID
Primary 00868020000208

Customer Contacts

Phone
888-757-9355

Premarket Submissions

Submission Number Supplement Number
K102404 000

Device Sizes

Type Value Unit Text
Device Size Text, specify Expiratory Resistance 3.0 >= x < 8.0 cm H2O at 50 mL/sec flow rate per nostril

Storage Conditions

Type
Storage Environment Humidity
Temperature Range
0 – 40 Percent (%) Relative Humidity