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Schiller ECG patient cable

FDA UDI

Class II (US FDA UDI)

by Schiller Corp.

Identity

Trade Name
Schiller ECG patient cable FDA UDI
Generic Name
Electrocardiographic lead set, reusable FDA UDI
Device Name
ECG 10-wire patient cable IEC banana plug 2.0 m FDA UDI
Model / Reference
2.400216 FDA UDI
Description
ECG 10-wire patient cable IEC banana plug 2.0 m FDA UDI

Identifiers

Catalog Number
2.400216 FDA UDI
Primary DI / UDI-DI
07613365001808 FDA UDI
510(k) Number
K152043 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Electrocardiographic lead set, reusable

Schiller ECG patient cable by Schiller Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrocardiographic lead set, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Schiller Corp.

Sources (1)

  • FDA UDI 68917804-d50a-43d5-a74a-e2089cdcbc89 37 fields · synced May 30, 2026