3m™

FDA UDI

Class I (US FDA UDI)

by 3M Deutschland GmbH

Identity

Trade Name: 3M™ FDA UDI
Generic Name: Dental impression material syringe, reusable FDA UDI
Device Name: 3M™ Elastomer Syringe with Filling Device, 71209 FDA UDI
Model / Reference: 71209 FDA UDI
Description: 3M™ Elastomer Syringe with Filling Device, 71209 FDA UDI

Identifiers

Catalog Number: 71209 FDA UDI
Primary DI / UDI-DI: 04054596733671 FDA UDI
FDA Product Code: EID FDA UDI
GMDN Term: Dental impression material syringe, reusable 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

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Dental impression material syringe, reusable

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

Similar devices

Also classified as Dental impression material syringe, reusable.

Plasdent — PLASDENT CORP. · Class I
Plasdent — PLASDENT CORP. · Class I
Plasdent — PLASDENT CORP. · Class I
Astek — Young Innovations, Inc. · Class I
COE SYRINGE — Gc America Inc. · Class I
Astek — Young Innovations, Inc. · Class I
MASTER-DENT — DENTONICS, INC.
MASTER-DENT — DENTONICS, INC.

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

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

Manufacturer

Manufacturer: 3M Deutschland GmbH

Sources (1)

FDA UDI 38f7bd2a-9a89-4c75-8a2d-c8e2f5d60c28 35 fields · synced May 30, 2026