← Back to catalogue

DreamStation

FDA UDI

Class II (US FDA UDI)

by Respironics, Inc.

Identity

Trade Name
DreamStation FDA UDI
Generic Name
Home BPAP unit FDA UDI
Device Name
DreamStation Auto BiPAP with Humidifier, BL FDA UDI
Model / Reference
DreamStation Auto BiPAP with Humidifier, BL FDA UDI
Description
DreamStation Auto BiPAP with Humidifier, BL FDA UDI

Identifiers

Catalog Number
BLX700H15 FDA UDI
Primary DI / UDI-DI
00606959027992 FDA UDI
FDA Product Code
BZD FDA UDI
GMDN Term
Home BPAP unit FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Home BPAP unit

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

Similar devices

Also classified as Home BPAP unit.

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 ddfa1c56-f2e1-499a-81f4-cd7968e35cc0 36 fields · synced Jun 8, 2026