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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 skin pad, single-use FDA UDI
Device Name
PAD, DEFIB, PEDI, RADIOLUCENT, ZOLL FDA UDI
Model / Reference
MDSPEDZOL FDA UDI
Description
PAD, DEFIB, PEDI, RADIOLUCENT, ZOLL FDA UDI

Identifiers

Catalog Number
MDSPEDZOL FDA UDI
Primary DI / UDI-DI
10888277634954 FDA UDI
510(k) Number
K081442 FDA UDI
FDA Product Code
LDD FDA UDI
GMDN Term
Electrode conductive skin pad, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.5300 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

No

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 skin pad, single-use

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

Similar devices

Also classified as Electrode conductive skin pad, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 7de2f695-03df-4c51-9aec-f3189e7f72dd 36 fields · synced May 31, 2026