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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™ ESPE™ Polyether Tray Adhesive Refill, 30600 FDA UDI
Model / Reference
30600 FDA UDI
Description
3M™ ESPE™ Polyether Tray Adhesive Refill, 30600 FDA UDI

Identifiers

Catalog Number
30600 FDA UDI
Primary DI / UDI-DI
J001702011099750 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

No

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

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Manufacturer

Manufacturer
3M Deutschland GmbH

Sources (1)

  • FDA UDI f5b4d73e-27ee-4917-8c0c-64a3bc524cc5 35 fields · synced May 30, 2026