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Apk

FDA UDI

Class II (US FDA UDI)

by Apk Technology

Identity

Trade Name
APK FDA UDI
Generic Name
Electrocardiographic lead set, reusable FDA UDI
Device Name
inch, Disposable/SPU, Spacelabs & Philips Compatible, ECG Leadwire, AHA/AAMI FDA UDI
Model / Reference
M-PS-5PS-050 FDA UDI
Description
inch, Disposable/SPU, Spacelabs & Philips Compatible, ECG Leadwire, AHA/AAMI FDA UDI

Identifiers

Primary DI / UDI-DI
06946725544716 FDA UDI
FDA Product Code
DSA FDA UDI
GMDN Term
Electrocardiographic lead set, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2900 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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Electrocardiographic lead set, reusable

Apk by Apk Technology — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrocardiographic lead set, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Apk Technology

Sources (1)

  • FDA UDI a648a7b7-4f82-469d-a597-d8862da2db12 33 fields · synced May 31, 2026