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Extrude

FDA UDIEUDAMED

Class II (US FDA UDI)

Ref 29034

by Kerr Corporation

Identity

Trade Name
Extrude EUDAMEDFDA UDI
Generic Name
Silicone dental impression material FDA UDI
Device Name
Extrude EUDAMED
Value Pack - Polyvinylsiloxane Impression Material - Extra - Type 1: high consistency FDA UDI
Model / Reference
29034 EUDAMEDFDA UDI
Description
Value Pack - Polyvinylsiloxane Impression Material - Extra - Type 1: high consistency FDA UDI

Identifiers

Primary DI / UDI-DI
10841396116510 EUDAMEDFDA UDI
Basic UDI-DI
805151187100001657 EUDAMED
FDA Product Code
ELW FDA UDI
EMDN Code
Q01020199 DENTAL IMPRESSION MATERIALS - OTHER EUDAMED
GMDN Term
Silicone dental impression material FDA UDI

Classification

Device Class
Class I EUDAMED
Class II FDA UDI
Regulation Number
872.3660 FDA UDI
Market of Registration
Italy EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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: Silicone dental impression material

Extrude by Kerr Corporation — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Silicone dental impression material.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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

Manufacturer

Manufacturer
Kerr Corporation

Sources (2)

  • FDA UDI 7be6889f-e01b-4657-ad16-70b6e3674e6a 35 fields · synced Jul 12, 2026
  • EUDAMED 79161934-9174-4e14-8476-8ba2dd0e63cc 61 fields · synced Jul 12, 2026