FDA UDI In Commercial Distribution 🇺🇸 United States

ResScan

DI: 08401934313389 · Model: 31338 · RESMED CORP.
Product Codes
4
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ResScan
Primary DI
08401934313389
Version / Model
31338
Company Name
RESMED CORP.
Labeler DUNS
080243150
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-02-24
Public Version
2
Public Version Date
2023-03-08
Public Version Status
Update
Public Device Record Key
1e996737-6cf1-4d18-9370-366f96181cc6

Device Description

ResScan v7.0.1

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
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)
CBK Ventilator, Continuous, Facility Use
MNS Ventilator, Continuous, Non-Life-Supporting
MNT Ventilator, Continuous, Minimal Ventilatory Support, Facility Use

GMDN Terms

Code Name
40582 Ventilator application software

Identifiers

Type ID
Primary 08401934313389

Customer Contacts