FDA UDI In Commercial Distribution 🇺🇸 United States

ResMed

DI: 00619498272013 · Model: 27201 · RESMED PTY LTD
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ResMed
Primary DI
00619498272013
Version / Model
27201
Catalog Number
27201
Company Name
RESMED PTY LTD
Labeler DUNS
751149311
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-15
Public Version
3
Public Version Date
2021-07-23
Public Version Status
Update
Public Device Record Key
cb7d454d-b2ab-496b-a1f1-2bd95ac696fb

Device Description

Connectivity Module

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
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
Yes
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
OUG Medical Device Data System

GMDN Terms

Code Name
36862 Patient monitoring system module, interfacing

Identifiers

Type ID
Primary 00619498272013

Customer Contacts

Phone
800-424-0737

Storage Conditions

Type
Storage Environment Humidity
Temperature Range
10 – 95 Percent (%) Relative Humidity
Type
Storage Environment Temperature
Temperature Range
-4 – 140 Degrees Fahrenheit