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Easy Cube

FDA UDI

Class I (US FDA UDI)

by L A P Gmbh Laser Applikationen

Identity

Trade Name
EASY CUBE FDA UDI
Generic Name
Multi-modality therapeutic radiation phantom, anthropomorphic FDA UDI
Model / Reference
Spacer 20 x 20 x 20mm FDA UDI

Identifiers

Catalog Number
0014465 FDA UDI
Primary DI / UDI-DI
04260590371614 FDA UDI
FDA Product Code
LHO FDA UDI
GMDN Term
Multi-modality therapeutic radiation phantom, anthropomorphic FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
892.1940 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

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Multi-modality therapeutic radiation phantom, anthropomorphic

Easy Cube by L A P Gmbh Laser Applikationen — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Multi-modality therapeutic radiation phantom, anthropomorphic.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
L A P Gmbh Laser Applikationen

Sources (1)

  • FDA UDI 30ea7394-0293-4508-92da-48a32a2eb582 33 fields · synced May 30, 2026