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3m™

FDA UDI

Class II (US FDA UDI)

by 3M Deutschland GmbH

Identity

Trade Name
3M™ FDA UDI
Generic Name
Dental impression material adhesive FDA UDI
Device Name
3M™ ESPE™ VPS Tray Adhesive Refill, 7307 FDA UDI
Model / Reference
7307 FDA UDI
Description
3M™ ESPE™ VPS Tray Adhesive Refill, 7307 FDA UDI

Identifiers

Catalog Number
7307 FDA UDI
Primary DI / UDI-DI
J001702011064920 FDA UDI
FDA Product Code
ELW FDA UDI
GMDN Term
Dental impression material adhesive FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3660 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 impression material adhesive

3m™ by 3M Deutschland GmbH — Class II — 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 ff9ef28f-3f85-4be9-8dae-7d3874ae8d2c 35 fields · synced May 30, 2026