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Medline Industries, Inc.

FDA UDI

Class II (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
MEDLINE INDUSTRIES, INC. FDA UDI
Generic Name
Single-chamber venous compression system garment, single-use FDA UDI
Device Name
DBD-GARMENT,MEDLINE,DVT,SQ,CALF,SM,NO TR FDA UDI
Model / Reference
MDS601PSQ2 FDA UDI
Description
DBD-GARMENT,MEDLINE,DVT,SQ,CALF,SM,NO TR FDA UDI

Identifiers

Catalog Number
MDS601PSQ2 FDA UDI
Primary DI / UDI-DI
10888277414327 FDA UDI
FDA Product Code
JOW FDA UDI
GMDN Term
Single-chamber venous compression system garment, single-use 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: Single-chamber venous compression system garment, single-use

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

Similar devices

Also classified as Single-chamber venous compression system garment, single-use.

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 aa7610a3-ba13-4ab0-a9be-ba624c353cd0 35 fields · synced Jun 6, 2026