FDA UDI Not in Commercial Distribution 🇺🇸 United States

TUB10

DI: 36642240000232 · Model: TUB10 · Inogen, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
TUB10
Primary DI
36642240000232
Version / Model
TUB10
Catalog Number
TUB-10
Company Name
Inogen, Inc.
Labeler DUNS
136729634
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-03-12
Public Version
3
Public Version Date
2025-08-20
Public Version Status
Update
Public Device Record Key
f6503d2b-b5ae-4bf4-a4ce-6e8303d0539e
Distribution End Date
2025-03-12

Device Description

1 single patient use expiratory kit, composed of 1 tube, 1 filter programmed to allow 10 therapy sessions and 10 disposable mouthpieces

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
MR Unsafe
Direct Marking Exempt
Yes
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
SDT Intra-Pulmonary Percussive Vibration (Ipv) Devices

GMDN Terms

Code Name
48000 Vacuum-assisted airway secretion-clearing system

Identifiers

Type ID
Primary 36642240000232

Storage Conditions

Type
Storage Environment Atmospheric Pressure
Temperature Range
70 – 106 KiloPascal
Type
Storage Environment Humidity
Temperature Range
15 – 93 Percent (%) Relative Humidity
Type
Storage Environment Temperature
Temperature Range
-25 – 55 Degrees Celsius