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Medline

FDA UDI

Class II (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
Medline FDA UDI
Generic Name
Sharps container FDA UDI
Device Name
CONTAINER,SHARPS,1 QT.,RED,PHLEB. FDA UDI
Model / Reference
MDS705110 FDA UDI
Description
CONTAINER,SHARPS,1 QT.,RED,PHLEB. FDA UDI

Identifiers

Catalog Number
MDS705110 FDA UDI
Primary DI / UDI-DI
10080196282647 FDA UDI
FDA Product Code
MMK FDA UDI
GMDN Term
Sharps container FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5570 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: Sharps container

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

Similar devices

Also classified as Sharps container.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 16558c7d-eb32-4eec-950f-b662dded5f00 35 fields · synced Jun 1, 2026