← Back to catalogue

3m™

FDA UDI

Class I (US FDA UDI)

by 3M Deutschland GmbH

Identity

Trade Name
3M™ FDA UDI
Generic Name
Dental impression material adhesive FDA UDI
Device Name
3M™ Polyether Contact Tray Adhesive Refill, 69408 FDA UDI
Model / Reference
69408 FDA UDI
Description
3M™ Polyether Contact Tray Adhesive Refill, 69408 FDA UDI

Identifiers

Catalog Number
69408 FDA UDI
Primary DI / UDI-DI
04054596648791 FDA UDI
FDA Product Code
EBH FDA UDI
GMDN Term
Dental impression material adhesive FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3670 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

Yes

FDA UDI

Category: Dental impression material adhesive

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 adhesive.

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 195cd6c0-fd44-42f2-9449-d5d954495410 35 fields · synced May 30, 2026