FDA UDI In Commercial Distribution 🇺🇸 United States

AirTouch N30I

DI: 00619498623099 · Model: 62309 · RESMED PTY LTD
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
AirTouch N30I
Primary DI
00619498623099
Version / Model
62309
Catalog Number
62309
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
deb5cd7e-b4b2-4f63-8d58-0f60b0844434

Device Description

AIRTOUCH N30I SML STPK V2

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
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 00619498623099

Customer Contacts

Phone
800-424-0737

Storage Conditions

Type
Storage Environment Humidity
Temperature Range
0 – 95 Degrees Celsius
Type
Storage Environment Temperature
Temperature Range
-4 – 140 Degrees Fahrenheit