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Vng

FDA UDI

Class II (US FDA UDI)

by Inventis Srl

Identity

Trade Name
VNG FDA UDI
Generic Name
Dynamic visual acuity testing system FDA UDI
Device Name
Video nystagmograph FDA UDI
Model / Reference
VIDEO-SCOPE WIRED FDA UDI
Description
Video nystagmograph FDA UDI

Identifiers

Catalog Number
11961 FDA UDI
Primary DI / UDI-DI
08054187381065 FDA UDI
FDA Product Code
GWN FDA UDI
GMDN Term
Dynamic visual acuity testing system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.1460 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

No

FDA UDI

Category: Dynamic visual acuity testing system

Vng by Inventis Srl — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dynamic visual acuity testing system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Inventis Srl

Sources (1)

  • FDA UDI 710cc80a-5fc6-4c36-bc49-c2624818b7c4 35 fields · synced Jun 1, 2026