Unimed

FDA UDI

Class II (US FDA UDI)

by Unimed Medical Supplies, Inc.

Identity

Trade Name: Unimed FDA UDI
Generic Name: Electrocardiographic lead set, single-use FDA UDI
Device Name: Disposable ECG Lead Wires/MQ style/5-lead/Snap/AHA/0.9M/Pacific FDA UDI
Model / Reference: NLMQ5252-X FDA UDI
Description: Disposable ECG Lead Wires/MQ style/5-lead/Snap/AHA/0.9M/Pacific FDA UDI

Identifiers

Primary DI / UDI-DI: 06945664839105 FDA UDI
FDA Product Code: DSA FDA UDI
GMDN Term: Electrocardiographic lead set, single-use 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

Yes

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Electrocardiographic lead set, single-use

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

Similar devices

Also classified as Electrocardiographic lead set, single-use.

APK — Apk Technology · Class II
Philips — Apk Technology · Class II
Med-Dyne — MED-DYNE · Class II
SureLead — Authentic Medical · Class II
9Line — RISING EAGLE MEDICAL · Class II
Med-Dyne — MED-DYNE · Class II
Multi-Link™ — Airlife, Inc. · Class II
Med-Dyne — MED-DYNE · 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

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

Manufacturer

Manufacturer: Unimed Medical Supplies, Inc.

Sources (1)

FDA UDI e9b0d517-7b91-408d-956e-654e94420223 33 fields · synced May 30, 2026