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RotoMix™

FDA UDI

Class I (US FDA UDI)

by 3M Deutschland GmbH

Identity

Trade Name
RotoMix™ FDA UDI
Generic Name
Dental amalgam mixer FDA UDI
Device Name
3M™ ESPE™ Rotomix™ Capsule Mixing Unit, 120V/60Hz, 76310 FDA UDI
Model / Reference
76310 FDA UDI
Description
3M™ ESPE™ Rotomix™ Capsule Mixing Unit, 120V/60Hz, 76310 FDA UDI

Identifiers

Catalog Number
76310 FDA UDI
Primary DI / UDI-DI
J001702011022020 FDA UDI
FDA Product Code
EFD FDA UDI
GMDN Term
Dental amalgam mixer FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3100 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

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dental amalgam mixer

RotoMix™ by 3M Deutschland GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental amalgam mixer.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
3M Deutschland GmbH

Sources (1)

  • FDA UDI aadd85b6-92af-4447-ae9e-d3a993642ed0 35 fields · synced May 31, 2026