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Vng 3d

FDA UDI

Class II (US FDA UDI)

by Ecleris

Identity

Trade Name
VNG 3D FDA UDI
Generic Name
Electronystagmograph FDA UDI
Device Name
VIDEONISTAGMOGRAPHY SYSTEM FDA UDI
Model / Reference
RX1 FDA UDI
Description
VIDEONISTAGMOGRAPHY SYSTEM FDA UDI

Identifiers

Catalog Number
VN1061 FDA UDI
Primary DI / UDI-DI
B366VN1061 FDA UDI
510(k) Number
K130201 FDA UDI
FDA Product Code
GWN FDA UDI
GMDN Term
Electronystagmograph 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

No

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: Electronystagmograph

Vng 3d by Ecleris — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electronystagmograph.

Cleared under the same submission

K130201 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Ecleris

Sources (1)

  • FDA UDI 7af321c4-ed7d-47ec-bdcf-d55009a03adc 37 fields · synced May 30, 2026