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MaxView 4K, Lateral Imager

FDA UDI

Class I (US FDA UDI)

by Viseon, Inc.

Identity

Trade Name
MaxView 4K, Lateral Imager FDA UDI
Generic Name
General-purpose surgical microscope FDA UDI
Device Name
MaxView 4K, Lateral Imager, Long FDA UDI
Model / Reference
MAX-L20 FDA UDI
Description
MaxView 4K, Lateral Imager, Long FDA UDI

Identifiers

Primary DI / UDI-DI
00850007069490 FDA UDI
FDA Product Code
FSO FDA UDI
GMDN Term
General-purpose surgical microscope FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4700 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: General-purpose surgical microscope

MaxView 4K, Lateral Imager by Viseon, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General-purpose surgical microscope.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Viseon, Inc.

Sources (1)

  • FDA UDI 1f0c2525-e95b-43ba-9b77-7c3036d37812 33 fields · synced May 30, 2026