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Patterson®

FDA UDI

Class II (US FDA UDI)

by Patterson Dental Supply, Inc.

Identity

Trade Name
Patterson® FDA UDI
Generic Name
Composite dental impression material FDA UDI
Device Name
CEMENT, DENTAL FDA UDI
Model / Reference
71110618 FDA UDI
Description
CEMENT, DENTAL FDA UDI

Identifiers

Catalog Number
71110618 FDA UDI
Primary DI / UDI-DI
D66207111061807 FDA UDI
510(k) Number
K915618 FDA UDI
FDA Product Code
EMA FDA UDI
GMDN Term
Composite dental impression material FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3275 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

No

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: Composite dental impression material

Patterson® by Patterson Dental Supply, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Composite dental impression material.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI c9399cf0-219b-4c20-97f6-654aafa9bcdf 35 fields · synced May 30, 2026