← Back to catalogue

ALICE PDX Assembly, INTL

FDA UDI

Class II (US FDA UDI)

by Respironics, Inc.

Identity

Trade Name
ALICE PDX Assembly, INTL FDA UDI
Generic Name
Home-use sleep apnoea recording system FDA UDI
Device Name
Alice PDx Portable Sleep Diagnostics System, International FDA UDI
Model / Reference
INTERNATIONAL FDA UDI
Description
Alice PDx Portable Sleep Diagnostics System, International FDA UDI

Identifiers

Catalog Number
1043844X FDA UDI
Primary DI / UDI-DI
00606959060395 FDA UDI
510(k) Number
K090484 FDA UDI
FDA Product Code
MNR FDA UDI
GMDN Term
Home-use sleep apnoea recording system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.2375 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
MRI Safety
MR Unsafe FDA UDI

Category: Home-use sleep apnoea recording system

ALICE PDX Assembly, INTL by Respironics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Home-use sleep apnoea recording system.

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 4cb9f8db-4c36-49d0-82b2-cb11b0c04836 37 fields · synced Jun 6, 2026