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Alice PDx ECG Yoke, INTL

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref 1040810

by Respironics Inc.

Identity

Trade Name
Alice PDx ECG Yoke, INTL EUDAMED
Alice PDx FDA UDI
Generic Name
Home-use sleep apnoea recording system FDA UDI
Device Name
Alice PDx System EUDAMED
Alice PDx, Cable, ECG Yoke, International FDA UDI
Model / Reference
1040810 EUDAMED
Alice PDx ECG Yoke, INTL FDA UDI
Description
Alice PDx, Cable, ECG Yoke, International FDA UDI

Identifiers

Catalog Number
1040810 FDA UDI
Primary DI / UDI-DI
00606959020450 EUDAMEDFDA UDI
Basic UDI-DI
B-00606959020450 EUDAMED
510(k) Number
K090484 FDA UDI
FDA Product Code
MNR FDA UDI
EMDN Code
Z12100501 POLYSOMNOGRAPHS EUDAMED
GMDN Term
Home-use sleep apnoea recording system FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
868.2375 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Alice PDx ECG Yoke, INTL by Respironics, Inc. — Class IIa — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDD

United States Pending data

FDA UDI

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Manufacturer

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

Sources (3)

  • EUDAMED d527e179-b060-43c5-a36d-5ab43e797f6e 61 fields · synced Jun 18, 2026
  • FDA UDI a61cc2c9-c3a0-43e8-b327-d4f509d5c5ee 37 fields · synced May 30, 2026
  • EUDAMED 10e769f3-e1fb-402a-8149-4d202925de1d 61 fields · synced Jun 18, 2026