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VS3 Iridium

FDA UDI

Class II (US FDA UDI)

by Visionsense Ltd.

Identity

Trade Name
VS3 Iridium FDA UDI
Generic Name
Endoscope video camera FDA UDI
Device Name
VS3 Iridium Endoscope-IR 10mm, Long, 0°, Standard FOV - Refurbished FDA UDI
Model / Reference
153-0073RFB FDA UDI
Description
VS3 Iridium Endoscope-IR 10mm, Long, 0°, Standard FOV - Refurbished FDA UDI

Identifiers

Catalog Number
153-0073RFB FDA UDI
Primary DI / UDI-DI
10813040013261 FDA UDI
FDA Product Code
GWG FDA UDI
OWN FDA UDI
GCJ FDA UDI
HRX FDA UDI
GMDN Term
Endoscope video camera FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.1480 FDA UDI
876.1500 FDA UDI
888.1100 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: Endoscope video camera

VS3 Iridium by Visionsense Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endoscope video camera.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Visionsense Ltd.

Sources (1)

  • FDA UDI 96f26f92-c59a-457c-85ae-4250cf623856 34 fields · synced Jun 1, 2026