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EVIS EXERA lll COLONOVIDEOSCOPE

FDA UDI

Class II (US FDA UDI)

by Olympus Medical Systems Corporation

Identity

Trade Name
EVIS EXERA lll COLONOVIDEOSCOPE FDA UDI
Generic Name
Flexible video colonoscope, reusable FDA UDI
Device Name
CF-HQ190L EVIS EXERA III HD COLONOSCOPE FDA UDI
Model / Reference
OLYMPUS CF-HQ190L FDA UDI
Description
CF-HQ190L EVIS EXERA III HD COLONOSCOPE FDA UDI

Identifiers

Catalog Number
N3802140 FDA UDI
Primary DI / UDI-DI
04953170305115 FDA UDI
510(k) Number
K131780 FDA UDI
FDA Product Code
FDF FDA UDI
FDS FDA UDI
NWB FDA UDI
GMDN Term
Flexible video colonoscope, reusable 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: Flexible video colonoscope, reusable

EVIS EXERA lll COLONOVIDEOSCOPE by Olympus Medical Systems Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Flexible video colonoscope, reusable.

Cleared under the same submission

K131780 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Olympus Medical Systems Corporation

Sources (1)

  • FDA UDI 021bed89-5480-427d-b2d1-a5da08e909a5 36 fields · synced Jun 1, 2026