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Medline Renewal

FDA UDI

Class II (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
MEDLINE RENEWAL FDA UDI
Generic Name
External orthopaedic fixation system reprocessed component FDA UDI
Device Name
IMPAD RIGID SOLE FOOT COVER LARGE FDA UDI
Model / Reference
5075R FDA UDI
Description
IMPAD RIGID SOLE FOOT COVER LARGE FDA UDI

Identifiers

Catalog Number
5075R FDA UDI
Primary DI / UDI-DI
10888277374409 FDA UDI
FDA Product Code
JOW FDA UDI
GMDN Term
External orthopaedic fixation system reprocessed component FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.5800 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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: External orthopaedic fixation system reprocessed component

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

Similar devices

Also classified as External orthopaedic fixation system reprocessed component.

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 4f9f99d2-b65a-4192-8e0e-8c17e868a3d5 35 fields · synced May 31, 2026