FDA UDI In Commercial Distribution 🇺🇸 United States

AirTouch F30i

DI: 00619498624829 · Model: 62482 · RESMED PTY LTD
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
AirTouch F30i
Primary DI
00619498624829
Version / Model
62482
Company Name
RESMED PTY LTD
Labeler DUNS
751149311
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-10-09
Public Version
1
Public Version Date
2025-10-17
Public Version Status
New
Public Device Record Key
c508b297-4670-4eca-a6b8-80a3a52a0b5c

Device Description

AirTouch F30i CLR NO HG - L/STD

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
Yes
MRI Safety
MR Unsafe
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
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
BZD Ventilator, Non-Continuous (Respirator)

GMDN Terms

Code Name
57814 CPAP/BPAP face mask, reusable

Identifiers

Type ID
Primary 00619498624829

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
-4 – 140 Degrees Fahrenheit
Type
Storage Environment Humidity
Temperature Range
0 – 95 Percent (%) Relative Humidity