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Printed Model Analog

FDA UDI

Class I (US FDA UDI)

by Elos Medtech Pinol A/S

Identity

Trade Name
Printed Model Analog FDA UDI
Generic Name
Dental implant analog FDA UDI
Device Name
The product consists of the Elos Accurate® Analog for Printed Models (Analog) manufactured in the biocompatible material titanium alloy grade 5 ELI (TiAl6V4 ELI). FDA UDI
Model / Reference
68020087 FDA UDI
Description
The product consists of the Elos Accurate® Analog for Printed Models (Analog) manufactured in the biocompatible material titanium alloy grade 5 ELI (TiAl6V4 ELI). FDA UDI

Identifiers

Catalog Number
68020087 FDA UDI
Primary DI / UDI-DI
05712821012302 FDA UDI
FDA Product Code
NDP FDA UDI
GMDN Term
Dental implant analog FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3980 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Dental implant analog

Printed Model Analog by Elos Medtech Pinol A/S — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental implant analog.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI e77bc787-4963-4ee6-a63f-2b13412b2e06 35 fields · synced May 31, 2026