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Medline

FDA UDI

Class II (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
Medline FDA UDI
Generic Name
Multifunction cardiac electrode, paediatric FDA UDI
Device Name
ELECTRODE,PEDIATRIC,RT,FOAM,50PK FDA UDI
Model / Reference
MDSM6112250R FDA UDI
Description
ELECTRODE,PEDIATRIC,RT,FOAM,50PK FDA UDI

Identifiers

Catalog Number
MDSM6112250R FDA UDI
Primary DI / UDI-DI
10884389830215 FDA UDI
FDA Product Code
DRX FDA UDI
GMDN Term
Multifunction cardiac electrode, paediatric 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: Multifunction cardiac electrode, paediatric

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

Similar devices

Also classified as Multifunction cardiac electrode, paediatric.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medline Industries, Inc.

Sources (1)

  • FDA UDI 411b6ef2-1629-415d-baf2-193dcca52423 36 fields · synced Jun 6, 2026