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Dyevert™ Plus Ez

FDA UDI

Class II (US FDA UDI)

by Osprey Medical, Inc.

Identity

Trade Name
DYEVERT™ PLUS EZ FDA UDI
Generic Name
Contrast medium conservation system FDA UDI
Device Name
DyeVert Plus EZ Contrast Reduction System FDA UDI
Model / Reference
LV-EZ-PRS FDA UDI
Description
DyeVert Plus EZ Contrast Reduction System FDA UDI

Identifiers

Primary DI / UDI-DI
00815241020720 FDA UDI
FDA Product Code
DXT FDA UDI
GMDN Term
Contrast medium conservation system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1650 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Contrast medium conservation system

Dyevert™ Plus Ez by Osprey Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Contrast medium conservation system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Osprey Medical, Inc.

Sources (1)

  • FDA UDI 623b91d7-1c3d-406d-8677-092e97da1108 34 fields · synced Jun 1, 2026