← Back to catalogue

CuratOR

FDA UDI

Class II (US FDA UDI)

by Eizo Corporation

Identity

Trade Name
CuratOR FDA UDI
Generic Name
Endoscopic video image display unit FDA UDI
Device Name
32-inch 4K monitor FDA UDI
Model / Reference
EX3242 FDA UDI
Description
32-inch 4K monitor FDA UDI

Identifiers

Catalog Number
EX3242-FDWT FDA UDI
Primary DI / UDI-DI
04995047065968 FDA UDI
510(k) Number
K231066 FDA UDI
FDA Product Code
GCJ FDA UDI
GMDN Term
Endoscopic video image display unit FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 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: Endoscopic video image display unit

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

Similar devices

Also classified as Endoscopic video image display unit.

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
Eizo Corporation

Sources (1)

  • FDA UDI c5ce8f29-0b93-4e38-a4d8-ccb6b5744752 36 fields · synced May 31, 2026