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X-MIND trium

FDA UDI

Class II (US FDA UDI)

by De Götzen Srl

Identity

Trade Name
X-MIND trium FDA UDI
Generic Name
Stationary panoramic/tomographic dental x-ray system, digital FDA UDI
Device Name
X-MIND trium PAN_CEPH version including one removable ceph sensor, with control panel on the left and ceph arm on the right FDA UDI
Model / Reference
XMT PAN L CEPH R FDA UDI
Description
X-MIND trium PAN_CEPH version including one removable ceph sensor, with control panel on the left and ceph arm on the right FDA UDI

Identifiers

Catalog Number
W0900009 FDA UDI
Primary DI / UDI-DI
D804W09000090 FDA UDI
FDA Product Code
OAS FDA UDI
MUH FDA UDI
GMDN Term
Stationary panoramic/tomographic dental x-ray system, digital FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1750 FDA UDI
872.1800 FDA UDI
Commercial Distribution
Not 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

X-MIND trium by De Götzen Srl — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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 e89e443b-551d-46ae-9724-d509c2fe867a 37 fields · synced Jun 1, 2026