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Video Processor

FDA UDI

Class II (US FDA UDI)

by PENTAX of America, Inc.

Identity

Trade Name
VIDEO PROCESSOR FDA UDI
Generic Name
Endoscopic video image processing unit FDA UDI
Device Name
EPK-1000 VIDEO PROCESSOR (INTERNATIONAL USED) FDA UDI
Model / Reference
EPK-1000 FDA UDI
Description
EPK-1000 VIDEO PROCESSOR (INTERNATIONAL USED) FDA UDI

Identifiers

Primary DI / UDI-DI
04961333240180 FDA UDI
FDA Product Code
FET FDA UDI
GMDN Term
Endoscopic video image processing 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

No

FDA UDI

Category: Endoscopic video image processing unit

Video Processor by PENTAX of America, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endoscopic video image processing unit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 85c23344-ed45-4756-a7df-b12d6936a8a0 33 fields · synced May 29, 2026