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3M™ Aplicap™

FDA UDI

Class I (US FDA UDI)

by 3M Deutschland GmbH

Identity

Trade Name
3M™ Aplicap™ FDA UDI
Generic Name
Dental material cartridge-plunging applicator, two-component, manual FDA UDI
Device Name
3M™ Aplicap™ Activator/Applier Set, 37160 FDA UDI
Model / Reference
37160 FDA UDI
Description
3M™ Aplicap™ Activator/Applier Set, 37160 FDA UDI

Identifiers

Catalog Number
37160 FDA UDI
Primary DI / UDI-DI
04064035071950 FDA UDI
FDA Product Code
EID FDA UDI
GMDN Term
Dental material cartridge-plunging applicator, two-component, manual FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Dental material cartridge-plunging applicator, two-component, manual

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

Similar devices

Also classified as Dental material cartridge-plunging applicator, two-component, manual.

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 a2903a51-7031-4841-9c12-68d70dbc91a8 35 fields · synced May 30, 2026