FDA UDI In Commercial Distribution 🇺🇸 United States

AirFit X30i

DI: 00619498643561 · Model: 64356 · RESMED PTY LTD
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
AirFit X30i
Primary DI
00619498643561
Version / Model
64356
Company Name
RESMED PTY LTD
Labeler DUNS
751149311
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-12-09
Public Version
1
Public Version Date
2024-12-17
Public Version Status
New
Public Device Record Key
7f61e6c6-8332-423d-981f-3cb7f7b7641c

Device Description

AirFit X30i LGE STPK AMER - SLM

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
MR Unsafe
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
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 00619498643561
Direct Marking 00619498003006

Storage Conditions

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