3M™ ESPE™ Impregum™ Garant™

FDA UDI

Class I (US FDA UDI)

by 3M Deutschland GmbH

Identity

Trade Name: 3M™ ESPE™ Impregum™ Garant™ FDA UDI
Generic Name: Dental material mixing nozzle FDA UDI
Device Name: 3M™ ESPE™ Impregum™ Garant™ Soft Light Body Polyether Impression Material Refill, 31752 FDA UDI
Model / Reference: 31752 FDA UDI
Description: 3M™ ESPE™ Impregum™ Garant™ Soft Light Body Polyether Impression Material Refill, 31752 FDA UDI

Identifiers

Catalog Number: 31752 FDA UDI
Primary DI / UDI-DI: 04054596735750 FDA UDI
FDA Product Code: EID FDA UDI
ELW FDA UDI
GMDN Term: Dental material mixing nozzle FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 872.4565 FDA UDI
872.3660 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

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Dental material mixing nozzle Polyether dental impression material

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

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Also classified as Polyether dental impression material.

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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 I	Pending data

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Manufacturer

Manufacturer: 3M Deutschland GmbH

Sources (1)

FDA UDI 00343511-d540-4118-a1fa-0ca3f2b8976f 35 fields · synced Jun 8, 2026