FDA UDI In Commercial Distribution 🇺🇸 United States

AIRFIT F20

DI: 00619498161379 · Model: 16137 · RESMED PTY LTD
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
AIRFIT F20
Primary DI
00619498161379
Version / Model
16137
Catalog Number
16137
Company Name
RESMED PTY LTD
Labeler DUNS
751149311
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-11-16
Public Version
3
Public Version Date
2023-07-28
Public Version Status
Update
Public Device Record Key
77773433-7448-434a-bff2-df9e5b592d8c

Device Description

AIRFIT F20 LGE HEADGEAR - SLM

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
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
Direct Marking 00619498002986
Primary 00619498161379

Customer Contacts

Phone
800-424-0737

Storage Conditions

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