FDA UDI In Commercial Distribution 🇺🇸 United States

DreamMapper

DI: 00606959047501 · Model: 2.8 · Respironics, Inc.
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
DreamMapper
Primary DI
00606959047501
Version / Model
2.8
Catalog Number
1128265
Company Name
Respironics, Inc.
Labeler DUNS
080728314
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-06-21
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
1fc30c9b-194e-4af3-9022-d7f2f6ced71b

Device Description

DreamMapper Mobile Application Android (EMEA)

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
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 00606959047501

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K152356 000