← Back to catalogue

SilverRest Resting ECG TAB Electrode

FDA UDI

Class II (US FDA UDI)

by Graphic Controls Acquisition Corp

Identity

Trade Name
SilverRest Resting ECG TAB Electrode FDA UDI
Generic Name
Electrocardiographic electrode, single-use FDA UDI
Device Name
SilverRest Resting ECG TAB Electrode FDA UDI
Model / Reference
A10024 FDA UDI
Description
SilverRest Resting ECG TAB Electrode FDA UDI

Identifiers

Catalog Number
6500045V FDA UDI
Primary DI / UDI-DI
10009336010339 FDA UDI
FDA Product Code
DRX FDA UDI
GMDN Term
Electrocardiographic electrode, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2360 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Electrocardiographic electrode, single-use

SilverRest Resting ECG TAB Electrode by Graphic Controls Acquisition Corp — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrocardiographic electrode, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 71ffeba2-60fb-428a-95b1-76523a1f6c72 35 fields · synced Jun 1, 2026