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Impregum™ Penta™ Soft Heavy Body

FDA UDI

Class I (US FDA UDI)

by 3M Deutschland GmbH

Identity

Trade Name
Impregum™ Penta™ Soft Heavy Body FDA UDI
Generic Name
Dental impression material adhesive FDA UDI
Device Name
3M™ ESPE™ Impregum™ Penta™ Soft Heavy Body Polyether Impression Material Intro Kit, P31739 FDA UDI
Model / Reference
P31739 FDA UDI
Description
3M™ ESPE™ Impregum™ Penta™ Soft Heavy Body Polyether Impression Material Intro Kit, P31739 FDA UDI

Identifiers

Catalog Number
P31739 FDA UDI
Primary DI / UDI-DI
04035077005791 FDA UDI
FDA Product Code
EBH FDA UDI
ELW FDA UDI
EID FDA UDI
EFD FDA UDI
GMDN Term
Dental impression material adhesive FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3670 FDA UDI
872.3660 FDA UDI
872.4565 FDA UDI
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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dental material injection cannula, single-useDental material mixing nozzlePolyether dental impression materialDental impression material adhesive

Impregum™ Penta™ Soft Heavy Body by 3M Deutschland GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental impression material adhesive.

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 8d4cd9c5-d7fe-4175-994f-af52c0a1f2cd 35 fields · synced Jun 8, 2026