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Midmark ClearVision Digital Sensor System

FDA UDI

Class II (US FDA UDI)

by Midmark Corporation

Identity

Trade Name
Midmark ClearVision Digital Sensor System FDA UDI
Generic Name
Dental digital imaging sensor, intraoral FDA UDI
Device Name
Intraoral X-ray, Digital Imaging Sensor FDA UDI
Model / Reference
XSDS-01 FDA UDI
Description
Intraoral X-ray, Digital Imaging Sensor FDA UDI

Identifiers

Catalog Number
XSDS-01 FDA UDI
Primary DI / UDI-DI
00841709100406 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

Yes

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 ClearVision 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

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Manufacturer

Manufacturer
Midmark Corporation

Sources (1)

  • FDA UDI e307cf63-ac09-4964-af1b-0c0c3ba2b4d5 37 fields · synced Jun 8, 2026