Clarus Video Airway System

FDA UDI

Class II (US FDA UDI)

by Clarus Medical, Llc

Identity

Trade Name: Clarus Video Airway System FDA UDI
Generic Name: Flexible video laryngoscope FDA UDI
Device Name: Optical Stylet, , Video, Adult FDA UDI
Model / Reference: 30000-V FDA UDI
Description: Optical Stylet, , Video, Adult FDA UDI

Identifiers

Catalog Number: 30000-V FDA UDI
Primary DI / UDI-DI: B06730000V0 FDA UDI
510(k) Number: K082038 FDA UDI
FDA Product Code: EOB FDA UDI
GMDN Term: Flexible video laryngoscope FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 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

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

High-level Disinfectant FDA UDI

Category: Flexible video laryngoscope

Clarus Video Airway System by Clarus Medical, Llc — 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 - CERVICAL-STIM — Orthofix US LLC · Class III
RHINO-LARYNGO VIDEOSCOPE — Olympus Medical Systems Corporation · Class II
PEMF - PHYSIO-STIM — Orthofix US LLC · Class III
SourceMark — SOURCEMARK, LLC. · Class I
PEMF - PHYSIO-STIM — Orthofix US LLC · Class III

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: Clarus Medical, Llc

Sources (1)

FDA UDI e6b5279f-a438-40f2-a7ba-3061dfd4c4b9 36 fields · synced May 31, 2026