← Back to catalogue

U-Sense

FDA UDI

Class II (US FDA UDI)

by De Götzen Srl

Identity

Trade Name
U-SENSE FDA UDI
Generic Name
Dental digital imaging sensor, intraoral FDA UDI
Device Name
Intraoral Sensor U-SENSE size 2 FDA UDI
Model / Reference
U-SENSE SIZE 2 FDA UDI
Description
Intraoral Sensor U-SENSE size 2 FDA UDI

Identifiers

Catalog Number
W1300002 FDA UDI
Primary DI / UDI-DI
D804W13000020 FDA UDI
FDA Product Code
MUH FDA UDI
GMDN Term
Dental digital imaging sensor, intraoral 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: Dental digital imaging sensor, intraoral

U-Sense by De Götzen Srl — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental digital imaging sensor, intraoral.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
De Götzen Srl

Sources (1)

  • FDA UDI 8a1f6b65-cf5c-42f6-bd4e-37a6425ef599 36 fields · synced May 30, 2026