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Paradigm™ Temporization

FDA UDI

Class I (US FDA UDI)

by 3M Deutschland GmbH

Identity

Trade Name
Paradigm™ Temporization FDA UDI
Generic Name
Dental material mixing nozzle FDA UDI
Device Name
3M™ ESPE™ Paradigm™ Temporization Material, A1, 46993 FDA UDI
Model / Reference
46993 FDA UDI
Description
3M™ ESPE™ Paradigm™ Temporization Material, A1, 46993 FDA UDI

Identifiers

Catalog Number
46993 FDA UDI
Primary DI / UDI-DI
J001702011455810 FDA UDI
FDA Product Code
EID FDA UDI
EBG FDA UDI
GMDN Term
Dental material mixing nozzle FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4565 FDA UDI
872.3770 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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Temporary dental crown/bridgeDental material mixing nozzle

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

Similar devices

Also classified as Dental material mixing nozzle.

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 d9ae5bfa-bdae-4e5e-9700-1c67e176e1a3 35 fields · synced Jun 8, 2026