FDA UDI In Commercial Distribution 🇺🇸 United States

AIRTOUCH N30I

DI: 00619498623198 · Model: 62319 · RESMED PTY LTD
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
AIRTOUCH N30I
Primary DI
00619498623198
Version / Model
62319
Catalog Number
62319
Company Name
RESMED PTY LTD
Labeler DUNS
751149311
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-10-03
Public Version
1
Public Version Date
2024-10-11
Public Version Status
New
Public Device Record Key
b5a2be81-6f73-48f1-a25f-87a36f7c8bb3

Device Description

AIRTOUCH N30I FRAME SYS - SW/SML

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
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
57815 CPAP/BPAP nasal mask, reusable

Identifiers

Type ID
Primary 00619498623198

Customer Contacts

Phone
800-427-0737

Storage Conditions

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