3m™

FDA UDI

Class II (US FDA UDI)

by 3m Company

Identity

Trade Name: 3M™ FDA UDI
Generic Name: Dental milling system, CAD/CAM, chairside FDA UDI
Device Name: 3M™ True Definition Scanner, 78011 FDA UDI
Model / Reference: 78011 FDA UDI
Description: 3M™ True Definition Scanner, 78011 FDA UDI

Identifiers

Catalog Number: 78011 FDA UDI
Primary DI / UDI-DI: 30605861051478 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Dental milling system, CAD/CAM, chairside

3m™ by 3m Company — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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CS 3500 3D Scanner Collar — CARESTREAM HEALTH, INC. · Class II
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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: 3m Company

Sources (1)

FDA UDI 229bbe10-79b9-4328-bdb1-7e6187cc1c92 35 fields · synced May 30, 2026