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Midmark True Definition Scanner

FDA UDI

Class II (US FDA UDI)

by Midmark Corporation

Identity

Trade Name
Midmark True Definition Scanner FDA UDI
Generic Name
Dental milling system, CAD/CAM, chairside FDA UDI
Model / Reference
70-2014-0340-2 FDA UDI

Identifiers

Catalog Number
78032 FDA UDI
Primary DI / UDI-DI
00841709112027 FDA UDI
FDA Product Code
NOF FDA UDI
GMDN Term
Dental milling system, CAD/CAM, chairside FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3661 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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dental milling system, CAD/CAM, chairside

Midmark True Definition Scanner by Midmark Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental milling system, CAD/CAM, chairside.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Midmark Corporation

Sources (1)

  • FDA UDI 0196527d-bd66-4df1-a2b6-87e69955506d 34 fields · synced Jun 8, 2026