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Video Processor

FDA UDI

Class II (US FDA UDI)

by Cogentix Medical, Inc.

Identity

Trade Name
Video Processor FDA UDI
Generic Name
Endoscopic video image processing unit FDA UDI
Device Name
Digital Processing Unit - Reconditioned FDA UDI
Model / Reference
DPU-5050A FDA UDI
Description
Digital Processing Unit - Reconditioned FDA UDI

Identifiers

Catalog Number
07-5051P FDA UDI
Primary DI / UDI-DI
00874485002565 FDA UDI
510(k) Number
K072180 FDA UDI
FDA Product Code
FAJ 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
Not 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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Video Processor by Cogentix Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Cleared under the same submission

K072180 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cogentix Medical, Inc.

Sources (1)

  • FDA UDI eb9f852f-1cbd-4000-bc1a-3a1075cc9bea 37 fields · synced Jun 6, 2026