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Medline

FDA UDI

Class II (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
Medline FDA UDI
Generic Name
Electrical cable/lead holder FDA UDI
Device Name
LEADWIRE, CABLE, REUS, 5-LEAD, GE-DATEX FDA UDI
Model / Reference
MDSLWR104 FDA UDI
Description
LEADWIRE, CABLE, REUS, 5-LEAD, GE-DATEX FDA UDI

Identifiers

Catalog Number
MDSLWR104 FDA UDI
Primary DI / UDI-DI
10888277697683 FDA UDI
FDA Product Code
DSA FDA UDI
GMDN Term
Electrical cable/lead holder 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: Electrical cable/lead holder

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

Similar devices

Also classified as Electrical cable/lead holder.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI b7f08484-4a06-4f06-8075-e744ceaa5f9c 36 fields · synced Jun 8, 2026