FDA UDI In Commercial Distribution 🇺🇸 United States

DreamMapper

DI: 00606959046764 · Model: 2.7 · Respironics, Inc.
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
DreamMapper
Primary DI
00606959046764
Version / Model
2.7
Catalog Number
1101679
Company Name
Respironics, Inc.
Labeler DUNS
080728314
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-04-04
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
54643422-9caa-4d08-b6bf-dd5beadfa4a6

Device Description

DreamMapper Web

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 00606959046764

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K152356 000