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KING Shielded Acquisition Cable

FDA UDI

Class II (US FDA UDI)

by Kego Corporation

Identity

Trade Name
KING Shielded Acquisition Cable FDA UDI
Generic Name
Electrocardiographic lead set, reusable FDA UDI
Device Name
KING Shielded Acquisition Cable 5 PIN DIN Connector to 2 X Male Shrouded TP Connectors Red/Black Length 40” (102 cm) FDA UDI
Model / Reference
KM-PA05124RB FDA UDI
Description
KING Shielded Acquisition Cable 5 PIN DIN Connector to 2 X Male Shrouded TP Connectors Red/Black Length 40” (102 cm) FDA UDI

Identifiers

Primary DI / UDI-DI
00663427000338 FDA UDI
FDA Product Code
IKD FDA UDI
GMDN Term
Electrocardiographic lead set, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.1175 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

No

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

Yes

FDA UDI

Category: Electrocardiographic lead set, reusable

KING Shielded Acquisition Cable by Kego Corporation — 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
Kego Corporation

Sources (1)

  • FDA UDI d3b2332c-1804-461f-b9cc-3e3c4d4b45ad 33 fields · synced Jun 1, 2026