FDA UDI Not in Commercial Distribution 🇺🇸 United States

SIMEOX

DI: 36642240001604 · Model: SIMEOX · Inogen, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
SIMEOX
Primary DI
36642240001604
Version / Model
SIMEOX
Catalog Number
SIMEOX_H
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
655bdb9d-2cb2-4c2b-81e7-05cf941e3d9c
Distribution End Date
2025-03-12

Device Description

Simeox_H airway clearance device, with remote control, power supply, transport bag and user manual

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
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
SDT Intra-Pulmonary Percussive Vibration (Ipv) Devices

GMDN Terms

Code Name
48000 Vacuum-assisted airway secretion-clearing system

Identifiers

Type ID
Primary 36642240001604