Unimed

FDA UDI

Class II (US FDA UDI)

by Unimed Medical Supplies, Inc.

Identity

Trade Name: Unimed FDA UDI
Generic Name: Electrocardiographic lead set, reusable FDA UDI
Device Name: EKG Diagnosis Lead Wire for Mortara FDA UDI
Model / Reference: LMT10-LP-I0 FDA UDI
Description: EKG Diagnosis Lead Wire for Mortara FDA UDI

Identifiers

Primary DI / UDI-DI: 06936735492992 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Electrocardiographic lead set, reusable

Unimed by Unimed Medical Supplies, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Also classified as Electrocardiographic lead set, reusable.

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Multi-Link™ X2 Single-Patient-Use Direct-Connect Telemetry ECG Leadwire Set 3-Lead Set for Mindray, Snap, IEC — AirLife Finland Oy · Class I
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APK — Apk Technology · Class II
AMC — Advantage Medical Electronics, LLC · Class II

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Unimed Medical Supplies, Inc.

Sources (1)

FDA UDI 81c62383-ab28-4262-b41a-072a6a03d50f 33 fields · synced Jun 1, 2026