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Medichoice

FDA UDI

Class II (US FDA UDI)

by Owens & Minor Distribution, Inc.

Identity

Trade Name
Medichoice FDA UDI
Generic Name
Electrocardiographic lead set, single-use FDA UDI
Device Name
Cable Temp Adapter 2 Pin Round Plug To Dual Connector 3.0m Philips Compatible Reusable Not Made With Natural Rubber Latex MediChoice FDA UDI
Model / Reference
CL2407 FDA UDI
Description
Cable Temp Adapter 2 Pin Round Plug To Dual Connector 3.0m Philips Compatible Reusable Not Made With Natural Rubber Latex MediChoice FDA UDI

Identifiers

Primary DI / UDI-DI
10885632138638 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

No

FDA UDI

Single Use

No

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Electrocardiographic lead set, single-use

Medichoice by Owens & Minor Distribution, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrocardiographic lead set, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f6b3df75-bad4-4ac6-9ea5-fa99db7f294b 34 fields · synced Jun 1, 2026