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Medline

FDA UDI

Class II (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
Medline FDA UDI
Generic Name
Gravity enema set FDA UDI
Device Name
TRAY,FOLEY,SILI-ELAST,18FR,10ML,W/BAG FDA UDI
Model / Reference
DYND11865 FDA UDI
Description
TRAY,FOLEY,SILI-ELAST,18FR,10ML,W/BAG FDA UDI

Identifiers

Catalog Number
DYND11865 FDA UDI
Primary DI / UDI-DI
10080196991112 FDA UDI
FDA Product Code
OHR FDA UDI
GMDN Term
Gravity enema set 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

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

Dimensions & Sizes

Size
Catheter Gauge — 18 French FDA UDI
Total Volume — 10 Milliliter FDA UDI

Category: Gravity enema set

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

Similar devices

Also classified as Gravity enema set.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI ae46ee83-52e3-4df8-970b-8573614d4ebe 37 fields · synced May 30, 2026