FDA UDI In Commercial Distribution 🇺🇸 United States

AIRFIT P30i

DI: 00619498638567 · Model: 63856 · RESMED PTY LTD
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
AIRFIT P30i
Primary DI
00619498638567
Version / Model
63856
Catalog Number
63856
Company Name
RESMED PTY LTD
Labeler DUNS
751149311
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-06-26
Public Version
2
Public Version Date
2021-07-23
Public Version Status
Update
Public Device Record Key
ae1541a2-5e8c-4b74-95b5-5893904652ae

Device Description

AIRFIT P30I STD FRAME SYS - S

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
57815 CPAP/BPAP nasal mask, reusable

Identifiers

Type ID
Primary 00619498638567

Customer Contacts

Phone
800-424-0737

Storage Conditions

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