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Evis Exera Iii Gastrointestinal Videoscope

FDA UDI

Class II (US FDA UDI)

by Olympus Medical Systems Corporation

Identity

Trade Name
EVIS EXERA III GASTROINTESTINAL VIDEOSCOPE FDA UDI
Generic Name
Flexible video gastroduodenoscope FDA UDI
Model / Reference
OLYMPUS GIF-HQ190 FDA UDI

Identifiers

Catalog Number
N3802941 FDA UDI
Primary DI / UDI-DI
04953170436734 FDA UDI
FDA Product Code
FDF FDA UDI
GMDN Term
Flexible video gastroduodenoscope 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

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

Yes

FDA UDI

Category: Flexible video gastroduodenoscope

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

Similar devices

Also classified as Flexible video gastroduodenoscope.

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 0274d4ae-861f-4362-9cc0-e7e449611e04 34 fields · synced May 30, 2026