← Back to catalogue

Imprint™ 4 Regular

FDA UDI

Class II (US FDA UDI)

by 3M Deutschland GmbH

Identity

Trade Name
Imprint™ 4 Regular FDA UDI
Generic Name
Dental material mixing nozzle FDA UDI
Device Name
3M™ ESPE™ Imprint™ 4 Regular Sample Pack, 71519 FDA UDI
Model / Reference
71519 FDA UDI
Description
3M™ ESPE™ Imprint™ 4 Regular Sample Pack, 71519 FDA UDI

Identifiers

Catalog Number
71519 FDA UDI
Primary DI / UDI-DI
J001702011417620 FDA UDI
FDA Product Code
ELW FDA UDI
EID FDA UDI
GMDN Term
Dental material mixing nozzle FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3660 FDA UDI
872.4565 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: Silicone dental impression materialDental material mixing nozzle

Imprint™ 4 Regular by 3M Deutschland GmbH — Class II — 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
3M Deutschland GmbH

Sources (1)

  • FDA UDI a838a60a-8253-426b-ab41-f27b966e1fc9 35 fields · synced May 30, 2026