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
Device Name: RHINO-LARYNGO VIDEOSCOPE FDA UDI
Model / Reference: OLYMPUS ENF-VH FDA UDI
Description: RHINO-LARYNGO VIDEOSCOPE FDA UDI

Identifiers

Catalog Number: N6006840 FDA UDI
Primary DI / UDI-DI: 04953170411403 FDA UDI
510(k) Number: K221638 FDA UDI
FDA Product Code: NWB FDA UDI
EOB FDA UDI
GMDN Term: Flexible video laryngoscope FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 876.1500 FDA UDI
874.4760 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: 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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Also classified as Flexible video laryngoscope.

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PEMF - PHYSIO-STIM — Orthofix US LLC · Class III

Cleared under the same submission

K221638 also covers:

RHINO-LARYNGO VIDEOSCOPE — Olympus Medical Systems Corporation

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 31c9cfe3-0fb3-43cd-bc47-16161455172e 36 fields · synced May 30, 2026