FDA UDI In Commercial Distribution 🇺🇸 United States

AirFit F30

DI: 00619498641000 · Model: 64100 · RESMED PTY LTD
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
AirFit F30
Primary DI
00619498641000
Version / Model
64100
Catalog Number
64100
Company Name
RESMED PTY LTD
Labeler DUNS
751149311
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-10-15
Public Version
2
Public Version Date
2021-07-23
Public Version Status
Update
Public Device Record Key
6bfa9fd4-b860-472b-9dd7-d6361afb59fc

Device Description

AirFit F30 SML SYS

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
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
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 00619498641000

Customer Contacts

Phone
800-427-0737

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
-20 – 60 Degrees Celsius
Type
Storage Environment Atmospheric Pressure
Temperature Range
0 – 95 Percent (%) Relative Humidity