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E-Guide

FDA UDI

Class I (US FDA UDI)

by Envisiontec GmbH

Identity

Trade Name
E-Guide FDA UDI
Generic Name
Dental guided surgery reference plate FDA UDI
Device Name
E-Guide is a light-curing material for the additive manufacturing of individual dental surgical drill guides FDA UDI
Model / Reference
RES-01-3012 FDA UDI
Description
E-Guide is a light-curing material for the additive manufacturing of individual dental surgical drill guides FDA UDI

Identifiers

Catalog Number
RES-01-3012 FDA UDI
Primary DI / UDI-DI
04260683220133 FDA UDI
FDA Product Code
NDP FDA UDI
GMDN Term
Dental guided surgery reference plate 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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Dental guided surgery reference plate

E-Guide by Envisiontec GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental guided surgery reference plate.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Envisiontec GmbH

Sources (1)

  • FDA UDI 05882665-c3b9-4946-b9cc-c60f0bdbc77b 36 fields · synced May 30, 2026