FDA UDI In Commercial Distribution 🇺🇸 United States

DreamMapper

DI: 00606959057654 · Model: DreamMapper Mobile App Android, North America Instance - 2 · Respironics, Inc.
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
DreamMapper
Primary DI
00606959057654
Version / Model
DreamMapper Mobile App Android, North America Instance - 2
Catalog Number
1101479
Company Name
Respironics, Inc.
Labeler DUNS
080728314
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-09-03
Public Version
2
Public Version Date
2021-03-05
Public Version Status
Update
Public Device Record Key
ad62f133-662e-433c-bb3c-d5a1938a2082

Device Description

DreamMapper Mobile App Android (DMM)

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
No
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
BZD VENTILATOR, NON-CONTINUOUS (RESPIRATOR)
MNS VENTILATOR, CONTINUOUS, NON-LIFE-SUPPORTING
MNT Ventilator, continuous, minimal ventilatory support, facility use

GMDN Terms

Code Name
58884 Self-care monitoring/reporting software

Identifiers

Type ID
Primary 00606959057654