Esokid esophageal lead for cardiac recording and stimulation

Device name

—

Basic UDI-DI

803300326003000004KJ

Device model

Esokid esophageal lead for cardiac recording and stimulation

Issuing agency

GS1

Version date

Dec 18, 2025

Applicable legislation

MDR [Regulation (EU) 2017/745 on medical devices]

Risk category

Class IIa

Status

On the market

No device characteristics flagged

European Medical Device Nomenclature — the EU product classifications carried across this device family's references.

• C020203Transoesophageal recording and stimulation leads