← Back to catalogue

DreamMapper App iOS

FDA UDI

Class II (US FDA UDI)

by Respironics, Inc.

Identity

Trade Name
DreamMapper App iOS FDA UDI
Generic Name
Self-care monitoring/reporting software FDA UDI
Device Name
DreamMapper iOS NA Instance v 2.10 FDA UDI
Model / Reference
2.10 FDA UDI
Description
DreamMapper iOS NA Instance v 2.10 FDA UDI

Identifiers

Catalog Number
1101478 FDA UDI
Primary DI / UDI-DI
00606959049086 FDA UDI
510(k) Number
K152356 FDA UDI
FDA Product Code
MNT FDA UDI
BZD FDA UDI
MNS FDA UDI
GMDN Term
Self-care monitoring/reporting software FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5895 FDA UDI
868.5905 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Self-care monitoring/reporting software

DreamMapper App iOS by Respironics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Self-care monitoring/reporting software.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Respironics, Inc.

Sources (1)

  • FDA UDI cd373619-759e-4f3b-80c0-247987a8c1b1 35 fields · synced May 30, 2026