FDA UDI Not in Commercial Distribution 🇺🇸 United States

SIMEOX 200

DI: 36642240001840 · Model: SIMEOX-2 · Inogen, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
SIMEOX 200
Primary DI
36642240001840
Version / Model
SIMEOX-2
Catalog Number
ACD-200
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
9a51a816-81ed-49e7-9a30-225559cfb200
Distribution End Date
2025-03-12

Device Description

Simeox 200 airway clearance device, with remote control, power supply, transport bag and user manual. 3664224SIMEOX+KIT8F

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
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 36642240001840

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 – 70 Degrees Celsius