Virtuox

FDA UDI

Class II (US FDA UDI)

by Healthcare Logistics Systems

Identity

Trade Name: Virtuox FDA UDI
Generic Name: Pulse oximeter probe, reusable FDA UDI
Device Name: VPOD Capox, Adult Finger Clip Probe FDA UDI
Model / Reference: 1301 FDA UDI
Description: VPOD Capox, Adult Finger Clip Probe FDA UDI

Identifiers

Primary DI / UDI-DI: 00817698020131 FDA UDI
510(k) Number: K093016 FDA UDI
FDA Product Code: DQA FDA UDI
GMDN Term: Pulse oximeter probe, reusable FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 870.2700 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

FDA UDI

Category: Pulse oximeter probe, reusable

Virtuox by Healthcare Logistics Systems — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Also classified as Pulse oximeter probe, reusable.

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Unimed — Unimed Medical Supplies, Inc. · Class II
Unimed — Unimed Medical Supplies, Inc. · Class II
Unimed — Unimed Medical Supplies, Inc. · Class II

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: Healthcare Logistics Systems

Sources (1)

FDA UDI 2dd06dd8-3817-4a34-b417-7499aae9c03e 35 fields · synced May 30, 2026