FDA UDI In Commercial Distribution 🇺🇸 United States

AIRFIT F30I

DI: 00619498633739 · Model: 63373 · RESMED PTY LTD
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
AIRFIT F30I
Primary DI
00619498633739
Version / Model
63373
Catalog Number
63373
Company Name
RESMED PTY LTD
Labeler DUNS
751149311
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-06-03
Public Version
3
Public Version Date
2023-07-28
Public Version Status
Update
Public Device Record Key
42e4bea8-7bea-42b2-bdc1-8456480723df

Device Description

AIRFIT F30I SOFT WRAPS

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
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 00619498633739

Customer Contacts

Phone
8004240737

Storage Conditions

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