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Schiller ECG trunk cable

FDA UDI

Class II (US FDA UDI)

by Schiller Corp.

Identity

Trade Name
Schiller ECG trunk cable FDA UDI
Generic Name
Electrocardiographic lead set, reusable FDA UDI
Device Name
LP, IEC, 2.5m FDA UDI
Model / Reference
2.410202 FDA UDI
Description
LP, IEC, 2.5m FDA UDI

Identifiers

Catalog Number
2.400202 FDA UDI
Primary DI / UDI-DI
07613365000276 FDA UDI
510(k) Number
K012226 FDA UDI
K221056 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

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Electrocardiographic lead set, reusable

Schiller ECG trunk 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 d32b8e30-f0a0-434c-887f-304684a736ed 37 fields · synced May 30, 2026