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RadiForce®

FDA UDI

Class II (US FDA UDI)

by Eizo Corporation

Identity

Trade Name
RadiForce® FDA UDI
Generic Name
Image display unit, monochrome FDA UDI
Device Name
2MP Monochrome LCD Monitor FDA UDI
Model / Reference
GS220 FDA UDI
Description
2MP Monochrome LCD Monitor FDA UDI

Identifiers

Catalog Number
GS220-CL-BK-P FDA UDI
Primary DI / UDI-DI
04995047020561 FDA UDI
510(k) Number
K070131 FDA UDI
FDA Product Code
LLZ FDA UDI
GMDN Term
Image display unit, monochrome FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.2050 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

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: Image display unit, monochrome

RadiForce® by Eizo Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Image display unit, monochrome.

Cleared under the same submission

K070131 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Eizo Corporation

Sources (1)

  • FDA UDI 57e26c07-50cb-432b-9003-13b3bdb43a4d 36 fields · synced May 30, 2026