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Gastrointestinal Videoscope

FDA UDI

Class II (US FDA UDI)

by Olympus Medical Systems Corporation

Identity

Trade Name
GASTROINTESTINAL VIDEOSCOPE FDA UDI
Generic Name
Flexible video gastroduodenoscope FDA UDI
Model / Reference
OLYMPUS GIF-1100 FDA UDI

Identifiers

Catalog Number
N6019440 FDA UDI
Primary DI / UDI-DI
04953170420191 FDA UDI
510(k) Number
K222584 FDA UDI
FDA Product Code
FDF FDA UDI
FDS FDA UDI
NWB FDA UDI
FET FDA UDI
NTN 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

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.

Cleared under the same submission

K222584 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 e0b5db5b-4c20-485a-bb29-e14bb74fc9fa 35 fields · synced Jun 6, 2026