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KING Shielded Acq. Cable

FDA UDI

Class II (US FDA UDI)

by Kego Corporation

Identity

Trade Name
KING Shielded Acq. Cable FDA UDI
Generic Name
Electrocardiographic lead set, reusable FDA UDI
Device Name
KING Shielded Acq. Cable, 5 PIN DIN to 1 Red, 1 Green Alligator Clip, 1 1744 White Conn. 40" Qty1 FDA UDI
Model / Reference
KM-P050580RG FDA UDI
Description
KING Shielded Acq. Cable, 5 PIN DIN to 1 Red, 1 Green Alligator Clip, 1 1744 White Conn. 40" Qty1 FDA UDI

Identifiers

Primary DI / UDI-DI
00663427000598 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Electrocardiographic lead set, reusable

KING Shielded Acq. 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 a058fe45-b05e-4c17-a495-bab4b98f6900 33 fields · synced May 30, 2026