Vs3-Ir

FDA UDI

Class II (US FDA UDI)

by Visionsense Ltd.

Identity

Trade Name: VS3-IR FDA UDI
Generic Name: Endoscope video camera FDA UDI
Device Name: VS3 Iridium Endoscope-IR 5.5mm, Long, 30°, Standard FOV FDA UDI
Model / Reference: 153-0052 FDA UDI
Description: VS3 Iridium Endoscope-IR 5.5mm, Long, 30°, Standard FOV FDA UDI

Identifiers

Catalog Number: 153-0052 FDA UDI
Primary DI / UDI-DI: 18130400103427 FDA UDI
FDA Product Code: HRX FDA UDI
GCJ FDA UDI
GMDN Term: Endoscope video camera FDA UDI

Classification

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

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

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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: Visionsense Ltd.

Sources (1)

FDA UDI d40d5025-c1c7-43a9-834d-ca4c5bfd2ffd 34 fields · synced Jun 8, 2026