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Acarix CADScor Patch

FDA UDI

Class II (US FDA UDI)

by Acarix A/S

Identity

Trade Name
Acarix CADScor Patch FDA UDI
Generic Name
Phonocardiograph FDA UDI
Device Name
Acarix CADScor Patch, 20x patch in box. The intended use of the CADScor System is to record heart sounds, murmurs and vibration for calculation of a patient specific score, indicating the risk of coronary stenosis, as an aid in cardiac analysis and diagnosis. FDA UDI
Model / Reference
ACP-1401 FDA UDI
Description
Acarix CADScor Patch, 20x patch in box. The intended use of the CADScor System is to record heart sounds, murmurs and vibration for calculation of a patient specific score, indicating the risk of coronary stenosis, as an aid in cardiac analysis and diagnosis. FDA UDI

Identifiers

Catalog Number
ACP-1401 (20x) FDA UDI
Primary DI / UDI-DI
05700002223029 FDA UDI
510(k) Number
FDA Product Code
QMW FDA UDI
GMDN Term
Phonocardiograph FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1420 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Phonocardiograph

Acarix CADScor Patch by Acarix A/S — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Phonocardiograph.

Cleared under the same submission

DEN190047 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Acarix A/S

Sources (1)

  • FDA UDI 465f2081-31c7-406c-81fb-36f333081857 37 fields · synced Jun 8, 2026