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EasyDiagnost Eleva

FDA UDI

Class II (US FDA UDI)

by Philips Medical Systems GmbH, Dmc

Identity

Trade Name
EasyDiagnost Eleva FDA UDI
Generic Name
Stationary general-purpose fluoroscopic x-ray system, digital FDA UDI
Device Name
Table, Radiographic, Tilting FDA UDI
Model / Reference
9890-010-03632 FDA UDI
Description
Table, Radiographic, Tilting FDA UDI

Identifiers

Catalog Number
706050 FDA UDI
Primary DI / UDI-DI
00884838074255 FDA UDI
FDA Product Code
IXR FDA UDI
GMDN Term
Stationary general-purpose fluoroscopic x-ray system, digital FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1980 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

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

Yes

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

No

FDA UDI

Category: Stationary general-purpose fluoroscopic x-ray system, digital

EasyDiagnost Eleva by Philips Medical Systems GmbH, Dmc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Stationary general-purpose fluoroscopic x-ray system, digital.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Philips Medical Systems GmbH, Dmc

Sources (1)

  • FDA UDI 9b2bed23-ac15-4c28-b278-df275f1d0d91 34 fields · synced May 31, 2026