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Veraviewepocs

FDA UDI

Class II (US FDA UDI)

by J.morita Mfg.corp.

Identity

Trade Name
Veraviewepocs FDA UDI
Generic Name
Stationary panoramic/tomographic dental x-ray system, digital FDA UDI
Model / Reference
X550 FDA UDI

Identifiers

Primary DI / UDI-DI
04548213020379 FDA UDI
510(k) Number
K073696 FDA UDI
FDA Product Code
MUH FDA UDI
GMDN Term
Stationary panoramic/tomographic dental x-ray system, digital FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.1800 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

Yes

FDA UDI

Category: Stationary panoramic/tomographic dental x-ray system, digital

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

Similar devices

Also classified as Stationary panoramic/tomographic dental x-ray system, digital.

Cleared under the same submission

K073696 also covers:

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 9f7078a3-7493-4540-9d76-39652ff536ef 34 fields · synced May 30, 2026