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VistaIntra DC

FDA UDI

Class II (US FDA UDI)

by Vatech Co., Ltd.

Identity

Trade Name
VistaIntra DC FDA UDI
Generic Name
Hand-held intraoral dental x-ray system, digital FDA UDI
Device Name
Dental Extraoral Source X-ray System (Horizontal Arm Length 450mm) FDA UDI
Model / Reference
VistaIntra DC FDA UDI
Description
Dental Extraoral Source X-ray System (Horizontal Arm Length 450mm) FDA UDI

Identifiers

Primary DI / UDI-DI
08800016401882 FDA UDI
FDA Product Code
EHD FDA UDI
GMDN Term
Hand-held intraoral 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: Hand-held intraoral dental x-ray system, digital

VistaIntra DC by Vatech Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Hand-held intraoral dental x-ray system, digital.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Vatech Co., Ltd.

Sources (1)

  • FDA UDI e0fc1dca-7318-40d9-8489-43bf46ab3aab 34 fields · synced May 30, 2026