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Medline

FDA UDI

Class II (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
Medline FDA UDI
Generic Name
Single-chamber venous compression system garment, reusable FDA UDI
Device Name
GARMENT,MEDLINE,DVT,INT,THIGH,FOAM,LARGE FDA UDI
Model / Reference
MDS630LD FDA UDI
Description
GARMENT,MEDLINE,DVT,INT,THIGH,FOAM,LARGE FDA UDI

Identifiers

Catalog Number
MDS630LD FDA UDI
Primary DI / UDI-DI
10884389802786 FDA UDI
FDA Product Code
JOW FDA UDI
GMDN Term
Single-chamber venous compression system garment, reusable 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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Single-chamber venous compression system garment, reusable

Medline's Single-Chamber Venous Compression System is a reusable garment designed to promote venous blood flow, reducing the risk of oedema, DVT, and PE in non-ambulatory patients or those at high risk. Made from a single-chamber inflatable device, this medical device applies pressure through intermittent inflation, improving circulation and alleviating symptoms.

Similar devices

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI cf171357-1952-4d0c-a452-46a724710111 35 fields · synced Jul 23, 2026