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Vs3-Ir

FDA UDI

Class II (US FDA UDI)

by Visionsense Ltd.

Identity

Trade Name
VS3-IR FDA UDI
Generic Name
Endoscopic video image processing/light source system FDA UDI
Device Name
VS3 Iridium (785nm) – Visionsense 3DHD and IR Fluorescence Vision System, 110V FDA UDI
Model / Reference
145-0011 FDA UDI
Description
VS3 Iridium (785nm) – Visionsense 3DHD and IR Fluorescence Vision System, 110V FDA UDI

Identifiers

Catalog Number
145-0011 FDA UDI
Primary DI / UDI-DI
10813040013872 FDA UDI
FDA Product Code
OWN FDA UDI
GMDN Term
Endoscopic video image processing/light source system 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

Yes

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: Endoscopic video image processing/light source system

Vs3-Ir by Visionsense Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endoscopic video image processing/light source system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Visionsense Ltd.

Sources (1)

  • FDA UDI 0c7cccea-a1d1-4f3f-9507-c240b44b2f96 34 fields · synced May 30, 2026