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Veraview FX800

FDA UDI

Class II (US FDA UDI)

by J.morita Mfg.corp.

Identity

Trade Name
Veraview FX800 FDA UDI
Generic Name
Cone beam computed tomography system, head/neck FDA UDI
Model / Reference
X800N FDA UDI

Identifiers

Primary DI / UDI-DI
04548213053261 FDA UDI
510(k) Number
K201378 FDA UDI
FDA Product Code
OAS FDA UDI
GMDN Term
Cone beam computed tomography system, head/neck FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1750 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: Cone beam computed tomography system, head/neck

Veraview FX800 by J.morita Mfg.corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cone beam computed tomography system, head/neck.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
J.morita Mfg.corp.

Sources (1)

  • FDA UDI 558d3ad1-1c12-49d0-961b-f9989bb58e74 34 fields · synced Jun 6, 2026