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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 right and ceph arm on the right FDA UDI
Model / Reference
XMT PAN R CEPH R FDA UDI
Description
X-MIND trium PAN CEPH version including one removable ceph sensor, with control panel on the right and ceph arm on the right FDA UDI

Identifiers

Catalog Number
W0900230 FDA UDI
Primary DI / UDI-DI
D804W09002300 FDA UDI
510(k) Number
K160166 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 5341410a-7530-4bf3-80b8-4a1528d71cd0 38 fields · synced May 30, 2026