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Medline ReNewal

FDA UDI

Class II (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
Medline ReNewal FDA UDI
Generic Name
Single-chamber venous compression system garment, reprocessed FDA UDI
Device Name
MDS630BSQ VASO-FORCE SEQUENTIAL SLEEVE, FDA UDI
Model / Reference
REP115683 FDA UDI
Description
MDS630BSQ VASO-FORCE SEQUENTIAL SLEEVE, FDA UDI

Identifiers

Catalog Number
REP115683 FDA UDI
Primary DI / UDI-DI
10888277355330 FDA UDI
FDA Product Code
JOW FDA UDI
GMDN Term
Single-chamber venous compression system garment, reprocessed 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, reprocessed

Medline ReNewal 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, reprocessed.

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 2ed2a591-f840-494c-a7f4-7f59710431a9 36 fields · synced May 30, 2026