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X-MIND prime

FDA UDI

Class II (US FDA UDI)

by De Götzen Srl

Identity

Trade Name
X-MIND prime FDA UDI
Generic Name
Stationary panoramic/tomographic dental x-ray system, digital FDA UDI
Device Name
X-MIND prime CEPH version with double sensor open range FDA UDI
Model / Reference
XMP 2D CEPH DOUBLE SENSOR 110-240V FDA UDI
Description
X-MIND prime CEPH version with double sensor open range FDA UDI

Identifiers

Catalog Number
W1200009.DS FDA UDI
Primary DI / UDI-DI
D804W1200009DS0 FDA UDI
510(k) Number
K203374 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

X-MIND prime by De Götzen Srl — 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

K203374 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
De Götzen Srl

Sources (1)

  • FDA UDI c1c94e2c-454d-458b-86f9-579986fbe590 37 fields · synced May 31, 2026