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Medit Temporaries

FDA UDI

Class II (US FDA UDI)

by Medit Corp.

Identity

Trade Name
Medit Temporaries FDA UDI
Generic Name
CAD/CAM software FDA UDI
Device Name
SW Version: 1.1.x FDA UDI
Model / Reference
Medit Temporaries FDA UDI
Description
SW Version: 1.1.x FDA UDI

Identifiers

Primary DI / UDI-DI
08800026700180 FDA UDI
FDA Product Code
NOF FDA UDI
GMDN Term
CAD/CAM software 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

No

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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: CAD/CAM software

Medit Temporaries by Medit Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as CAD/CAM software.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medit Corp.

Sources (1)

  • FDA UDI 7117f39e-46e3-49c0-8f8f-7b971c264dde 33 fields · synced Jun 8, 2026