FDA UDI In Commercial Distribution 🇺🇸 United States

AIRFIT F40

DI: 00619498646029 · Model: 64602 · RESMED PTY LTD
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
AIRFIT F40
Primary DI
00619498646029
Version / Model
64602
Company Name
RESMED PTY LTD
Labeler DUNS
751149311
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-01-24
Public Version
1
Public Version Date
2024-02-01
Public Version Status
New
Public Device Record Key
33ea7ec2-a0b4-4e51-ab69-446e22721b7c

Device Description

AIRFIT F40 SYS - L/STD AMER

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 00619498646029

Customer Contacts

Phone
800-427-0737

Storage Conditions

Type
Storage Environment Humidity
Temperature Range
0 – 95 Percent (%) Relative Humidity
Type
Storage Environment Temperature
Temperature Range
-20 – 60 Degrees Celsius
Type
Storage Environment Temperature
Temperature Range
-4 – 140 Degrees Fahrenheit