Evis Exera Iii Video System Center

FDA UDI

Class II (US FDA UDI)

by Olympus Medical Systems Corporation

Identity

Trade Name: EVIS EXERA III VIDEO SYSTEM CENTER FDA UDI
Generic Name: Endoscopic video image processing unit FDA UDI
Device Name: CV-190 EVIS EXERA III VIDEO PROCESSOR FDA UDI
Model / Reference: OLYMPUS CV-190 FDA UDI
Description: CV-190 EVIS EXERA III VIDEO PROCESSOR FDA UDI

Identifiers

Primary DI / UDI-DI: 04953170298622 FDA UDI
510(k) Number: K121959 FDA UDI
K123365 FDA UDI
K131780 FDA UDI
FDA Product Code: NWB FDA UDI
FDF FDA UDI
FDS 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Endoscopic video image processing unit

Evis Exera Iii Video System Center by Olympus Medical Systems Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endoscopic video image processing unit.

Pixa — SANTA BARBARA IMAGING SYSTEMS, INC. · Class II
ILO — ILO electronic GmbH · Class I
AURORA® Surgiscope® — Integra Lifesciences Corp. · Class II
VIDEO PROCESSOR — PENTAX of America, Inc. · Class II
Digital Video Processor — Hunan Vathin Medical Instrument Co., Ltd · Class II
ILO — ILO electronic GmbH · Class I
3NT Video Console — 3nt Medical , Ltd. · Class II
HDMI cable — MacroLux Medical Technology Co., Ltd. · Class II

Cleared under the same submission

K121959 also covers:

K123365 also covers:

K131780 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer: Olympus Medical Systems Corporation

Sources (1)

FDA UDI 7ff0aeae-56f3-4530-9439-7050a8c57a7d 35 fields · synced Jun 8, 2026