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ECG Cable for SEER 1000

FDA UDI

Class II (US FDA UDI)

by getemed Medizin- und Informationstechnik AG

Identity

Trade Name
ECG Cable for SEER 1000 FDA UDI
Generic Name
Electrocardiographic lead set, reusable FDA UDI
Device Name
The cable is intended to be used to conduct electrical signals from a patient's heart, via an electrode attached to the surface of the chest/limbs, to an electrocardiograph (ECG) machine ( SEER 1000 recorder). FDA UDI
Model / Reference
5 Leads, 105 cm, AHA Color Code FDA UDI
Description
The cable is intended to be used to conduct electrical signals from a patient's heart, via an electrode attached to the surface of the chest/limbs, to an electrocardiograph (ECG) machine ( SEER 1000 recorder). FDA UDI

Identifiers

Catalog Number
2104816-001 FDA UDI
Primary DI / UDI-DI
04250903201646 FDA UDI
510(k) Number
K130785 FDA UDI
FDA Product Code
MWJ FDA UDI
GMDN Term
Electrocardiographic lead set, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2800 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

Yes

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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Electrocardiographic lead set, reusable

ECG Cable for SEER 1000 by getemed Medizin- und Informationstechnik AG — 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

Sources (1)

  • FDA UDI 0bca4828-9301-4c88-be96-007e3a128452 37 fields · synced Jun 1, 2026