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L.M.C Associates, Inc

FDA UDI

Class II (US FDA UDI)

by Graphic Controls Acquisition Corp

Identity

Trade Name
L.M.C Associates, Inc FDA UDI
Generic Name
Electrocardiographic electrode, single-use FDA UDI
Device Name
Radiolucent Foam Electrodes 60/pouch, 600 /case FDA UDI
Model / Reference
LMC 202 FDA UDI
Description
Radiolucent Foam Electrodes 60/pouch, 600 /case FDA UDI

Identifiers

Catalog Number
LMC 202 FDA UDI
Primary DI / UDI-DI
10813150022450 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

No

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Electrocardiographic electrode, single-use

L.M.C Associates, Inc 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

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Manufacturer

Manufacturer
Graphic Controls Acquisition Corp

Sources (1)

  • FDA UDI 2efda4b1-05f7-4be2-aeb9-dbe1522a0a8c 35 fields · synced May 29, 2026