← Back to catalogue

Dream Station Module

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 1147056

by Respironics Inc.

Identity

Trade Name
Dream Station Module EUDAMED
DreamStation SpO2 Connection Module EUDAMED
DreamStation FDA UDI
Generic Name
Clinical laboratory information system FDA UDI
Device Name
DreamStation Cell, Wi-Fi, and Link EUDAMED
DreamStation SpO2 Connection Module FDA UDI
Model / Reference
1147056 EUDAMED
DreamStation Spo2 Connection Module FDA UDI
Description
DreamStation SpO2 Connection Module FDA UDI

Identifiers

Catalog Number
1147056 FDA UDI
Primary DI / UDI-DI
00606959061132 EUDAMEDFDA UDI
Basic UDI-DI
0606959BM218LZ EUDAMED
FDA Product Code
OUG FDA UDI
EMDN Code
Z1203019080 VARIOUS INSTRUMENTS FOR ANAESTHESIA AND PULMONARY VENTILATION SUPPORT - HARDWARE ACCESSORIES EUDAMED
GMDN Term
Clinical laboratory information system FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
880.6310 FDA UDI
Market of Registration
Austria EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dream Station Module by Respironics, Inc. — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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

Manufacturer

Manufacturer
Respironics Inc.
EUDAMED SRN
US-MF-000002301
Authorised Representative
Respironics Deutschland GmbH & Co.KG DE-AR-000006164

Sources (3)

  • EUDAMED cfca5d7a-5f3b-478f-ac87-e4469d0ea674 61 fields · synced Jun 18, 2026
  • FDA UDI 6c17bc45-3326-4ddf-8e01-71a59f4b95ba 35 fields · synced May 30, 2026
  • EUDAMED 09b95fde-a9b8-47a5-ae0f-668cbf13cad8 61 fields · synced Jun 18, 2026