← Back to catalogue

Richmar Rex - Universal

FDA UDI

Class II (US FDA UDI)

by Compass Health Brands Corp.

Identity

Trade Name
RICHMAR REX - UNIVERSAL FDA UDI
Generic Name
Single-chamber venous compression system garment, reusable FDA UDI
Device Name
REX DVT System-Universal Pump, LE Garments & Backpack FDA UDI
Model / Reference
DVTREX-U FDA UDI
Description
REX DVT System-Universal Pump, LE Garments & Backpack FDA UDI

Identifiers

Primary DI / UDI-DI
00092237622926 FDA UDI
FDA Product Code
IRP FDA UDI
GMDN Term
Single-chamber venous compression system garment, reusable 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

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

Richmar Rex - Universal by Compass Health Brands Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Compass Health Brands Corp.

Sources (1)

  • FDA UDI 130c9984-4663-4114-9f05-129c8a57ad5f 34 fields · synced Jun 1, 2026