AirRay® Electrode Connection Cable US

FDA UDI

Class II (US FDA UDI)

by CorTec GmbH

Identity

Trade Name: AirRay® Electrode Connection Cable US FDA UDI
Generic Name: Analytical scalp lead FDA UDI
Model / Reference: Patient Cable 32 Channel FDA UDI

Identifiers

Catalog Number: 4031.1058.02 FDA UDI
Primary DI / UDI-DI: 04260656590072 FDA UDI
FDA Product Code: IKD FDA UDI
GMDN Term: Analytical scalp lead 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

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

MRI Safety

MR Unsafe FDA UDI

Category: Analytical scalp lead

AirRay® Electrode Connection Cable US by CorTec GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: CorTec GmbH

Sources (1)

FDA UDI 3786197f-2e09-476a-8032-fe30dd8bfc1e 35 fields · synced May 30, 2026