Rhino-Laryngo Videoscope

FDA UDI

Class II (US FDA UDI)

by Olympus Medical Systems Corporation

Identity

Trade Name: RHINO-LARYNGO VIDEOSCOPE FDA UDI
Generic Name: Flexible video laryngoscope FDA UDI
Model / Reference: ENF-VT3 FDA UDI

Identifiers

Primary DI / UDI-DI: 04953170411526 FDA UDI
510(k) Number: K183416 FDA UDI
FDA Product Code: EOB FDA UDI
NWB FDA UDI
GMDN Term: Flexible video laryngoscope FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 874.4760 FDA UDI
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

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: Flexible video laryngoscope

Rhino-Laryngo Videoscope by Olympus Medical Systems Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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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

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Manufacturer

Manufacturer: Olympus Medical Systems Corporation

Sources (1)

FDA UDI e0b39596-d24f-452c-a41a-4ef5f6894311 34 fields · synced May 30, 2026