← Back to catalogue

Midmark OptiMax Digital Sensor System

FDA UDI

Class II (US FDA UDI)

by Midmark Corporation

Identity

Trade Name
Midmark OptiMax Digital Sensor System FDA UDI
Generic Name
Dental digital imaging sensor, intraoral FDA UDI
Device Name
SENSOR SYSTEM CLEARVISION OPTIMAX, SIZE #1 AND SIZE #2, 3M CABLE FDA UDI
Model / Reference
XSDS-0C FDA UDI
Description
SENSOR SYSTEM CLEARVISION OPTIMAX, SIZE #1 AND SIZE #2, 3M CABLE FDA UDI

Identifiers

Catalog Number
XSDS-0C FDA UDI
Primary DI / UDI-DI
00841709104459 FDA UDI
510(k) Number
K112380 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

Midmark OptiMax Digital Sensor System by Midmark Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental digital imaging sensor, intraoral.

Cleared under the same submission

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
Midmark Corporation

Sources (1)

  • FDA UDI 36e4df24-7dda-4398-9e0f-e32c4276ea5e 37 fields · synced Jun 8, 2026