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Keeler Vantage Plus IO

FDA UDI

Class II (US FDA UDI)

by Quantel Medical

Identity

Trade Name
Keeler Vantage Plus IO FDA UDI
Generic Name
Indirect binocular laser ophthalmoscope FDA UDI
Device Name
Keeler Vantage Plus Indirect Ophthalmoscope FDA UDI
Model / Reference
LAFVP2 FDA UDI
Description
Keeler Vantage Plus Indirect Ophthalmoscope FDA UDI

Identifiers

Primary DI / UDI-DI
03700542625248 FDA UDI
FDA Product Code
HQF FDA UDI
GMDN Term
Indirect binocular laser ophthalmoscope FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
886.4390 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

No

FDA UDI

Category: Indirect binocular laser ophthalmoscope

Keeler Vantage Plus IO by Quantel Medical — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Indirect binocular laser ophthalmoscope.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Quantel Medical

Sources (1)

  • FDA UDI 136c367f-b786-409c-b836-051b15e192e9 34 fields · synced Jun 8, 2026