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Prosthetic Silicone Materials

FDA UDIEUDAMED

Class I (US FDA UDI)

Ref M514 (10)

by Technovent Limited

Identity

Trade Name
AntiSlump Agent - 10g EUDAMED
Prosthetic Silicone Materials FDA UDI
Generic Name
Dental appliance fabrication material, resin FDA UDI
Device Name
Prosthetic Silicone Materials EUDAMED
Silicone polymer-based additives designed to thicken uncured prosthetic silicones. FDA UDI
Model / Reference
M514 (10) EUDAMED
AntiSlump Agent - 10g FDA UDI
Description
Silicone polymer-based additives designed to thicken uncured prosthetic silicones. FDA UDI

Identifiers

Catalog Number
M514(10) FDA UDI
Primary DI / UDI-DI
05060483016269 EUDAMEDFDA UDI
Basic UDI-DI
506048301TF3D9 EUDAMED
Direct Marketing DI
05060483016269 EUDAMED
FDA Product Code
GBI FDA UDI
EMDN Code
Y0699 EXTERNAL PROSTHESES AND ORTHOSES - OTHER EUDAMED
GMDN Term
Dental appliance fabrication material, resin FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
878.3800 FDA UDI
Market of Registration
Malta 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

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

Yes

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 appliance fabrication material, resin

Prosthetic Silicone Materials by Technovent Limited — Class I — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Dental appliance fabrication material, resin.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Technovent Limited

Sources (2)

  • FDA UDI 4a2b0d75-9900-4f08-8dd8-728406846099 35 fields · synced Jul 30, 2026
  • EUDAMED ba0f4855-5b19-474e-ba44-18649fd3bc2c 61 fields · synced Jul 30, 2026