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Medline

FDA UDI

Class I (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
MEDLINE FDA UDI
Generic Name
Freestanding/bed-attached intravenous pole FDA UDI
Device Name
POLE,IV,HD,QUICK RELEASE CASTER,GRAY BSE FDA UDI
Model / Reference
MDS80600GRY FDA UDI
Description
POLE,IV,HD,QUICK RELEASE CASTER,GRAY BSE FDA UDI

Identifiers

Catalog Number
MDS80600GRY FDA UDI
Primary DI / UDI-DI
40080196666042 FDA UDI
FDA Product Code
FOX FDA UDI
GMDN Term
Freestanding/bed-attached intravenous pole FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6990 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

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Freestanding/bed-attached intravenous pole

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

Similar devices

Also classified as Freestanding/bed-attached intravenous pole.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 16d2dfce-56a7-4171-8ba4-43384a408f92 35 fields · synced Jun 8, 2026