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VersaVue Tablet - Global/CE Demo

FDA UDI

Class II (US FDA UDI)

by Medimaging Integrated Solution Inc.

Identity

Trade Name
VersaVue Tablet - Global/CE Demo FDA UDI
Generic Name
Flexible video cystoscope, single-use FDA UDI
Device Name
VersaVue Tablet - Global/CE Demo The VersaVue™ Tablet and VersaVue™ Video Box are plug-and-play visualization modules that are used with disposable VersaVue™ Cystoscopes to project images onto a monitor. FDA UDI
Model / Reference
5015 FDA UDI
Description
VersaVue Tablet - Global/CE Demo The VersaVue™ Tablet and VersaVue™ Video Box are plug-and-play visualization modules that are used with disposable VersaVue™ Cystoscopes to project images onto a monitor. FDA UDI

Identifiers

Catalog Number
M0067805100D FDA UDI
Primary DI / UDI-DI
04719872715320 FDA UDI
FDA Product Code
FAJ FDA UDI
GMDN Term
Flexible video cystoscope, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 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: Flexible video cystoscope, single-use

VersaVue Tablet - Global/CE Demo by Medimaging Integrated Solution Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Flexible video cystoscope, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI eee9d4e1-d0fc-4e1e-b8fa-7a2459ab4859 34 fields · synced May 31, 2026