FDA UDI In Commercial Distribution 🇺🇸 United States

AIRFIT F30I

DI: 00619498633333 · Model: 63333 · RESMED PTY LTD
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
AIRFIT F30I
Primary DI
00619498633333
Version / Model
63333
Catalog Number
63333
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
2def64e6-0c2d-47fa-9c86-a416f744c135

Device Description

AIRFIT F30I SYS - W/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
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 00619498633333

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