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Medline

FDA UDI

Class II (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
MEDLINE FDA UDI
Generic Name
Intermittent urethral catheterization kit FDA UDI
Device Name
TRAY,ERASECAUTI,INTERMIT FDA UDI
Model / Reference
URO4RR14C FDA UDI
Description
TRAY,ERASECAUTI,INTERMIT FDA UDI

Identifiers

Catalog Number
URO4RR14C FDA UDI
Primary DI / UDI-DI
10197344148998 FDA UDI
FDA Product Code
OHR FDA UDI
GMDN Term
Intermittent urethral catheterization kit FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.5130 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

Yes

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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: Intermittent urethral catheterization kit

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

Similar devices

Also classified as Intermittent urethral catheterization kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI c17b190b-6bb0-4306-bbbe-03cabe2a2017 36 fields · synced May 30, 2026