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Mueller Sports Medicine

FDA UDI

Class II (US FDA UDI)

by Mueller Sports Medicine, Inc.

Identity

Trade Name
Mueller Sports Medicine FDA UDI
Generic Name
Sequential venous compression system FDA UDI
Device Name
REVIVE HALF JACKET GRAY FDA UDI
Model / Reference
RG400 FDA UDI
Description
REVIVE HALF JACKET GRAY FDA UDI

Identifiers

Catalog Number
RG500 FDA UDI
Primary DI / UDI-DI
00074676007199 FDA UDI
510(k) Number
K163280 FDA UDI
FDA Product Code
IRP FDA UDI
GMDN Term
Sequential venous compression system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.5650 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

Yes

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Sequential venous compression system

Mueller Sports Medicine by Mueller Sports Medicine, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Sequential venous compression system.

Cleared under the same submission

K163280 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Mueller Sports Medicine, Inc.

Sources (1)

  • FDA UDI 9ae3bd2e-481e-4d11-a449-a467c56f794e 37 fields · synced Jun 9, 2026