FDA UDI Not in Commercial Distribution 🇺🇸 United States

Mobi

DI: 00619498003020 · Model: 35001 · RESMED PTY LTD
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Mobi
Primary DI
00619498003020
Version / Model
35001
Catalog Number
35001
Company Name
RESMED PTY LTD
Labeler DUNS
751149311
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-04-26
Public Version
3
Public Version Date
2023-07-31
Public Version Status
Update
Public Device Record Key
dc702be0-c045-4ef7-bfd6-4c704c2ad5e8
Distribution End Date
2023-07-30

Device Description

MOBI AMER1

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
No
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
CAW Generator, Oxygen, Portable

GMDN Terms

Code Name
12873 Stationary oxygen concentrator

Identifiers

Type ID
Primary 00619498003020

Storage Conditions

Type
Storage Environment Atmospheric Pressure
Temperature Range
70 – 101 KiloPascal
Type
Storage Environment Humidity
Temperature Range
15 – 93 Percent (%) Relative Humidity
Type
Storage Environment Temperature
Temperature Range
0 – 60 Degrees Celsius