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Medline

FDA UDI

Class II (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
Medline FDA UDI
Generic Name
Electrode conductive medium FDA UDI
Device Name
ELECTRODE,RADIOTRANSLUCENT,CLOTH,50PK FDA UDI
Model / Reference
MDSM611250R FDA UDI
Description
ELECTRODE,RADIOTRANSLUCENT,CLOTH,50PK FDA UDI

Identifiers

Catalog Number
MDSM611250R FDA UDI
Primary DI / UDI-DI
10884389830239 FDA UDI
FDA Product Code
DRX FDA UDI
GMDN Term
Electrode conductive medium 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

Category: Electrode conductive medium

Medline by Medline Industries, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrode conductive medium.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI aabb2a74-c9ed-4c26-a49d-2d522b74349b 36 fields · synced Jun 8, 2026