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CEREC Guide 3

FDA UDI

Class I (US FDA UDI)

by Sirona Dental Systems GmbH

Identity

Trade Name
CEREC Guide 3 FDA UDI
Generic Name
Dental guided surgery reference plate FDA UDI
Device Name
Guide Sleeve Ankylos ND / XiVe ND Guide Sleeve Ankylos ND / XiVe ND FDA UDI
Model / Reference
6669563 FDA UDI
Description
Guide Sleeve Ankylos ND / XiVe ND Guide Sleeve Ankylos ND / XiVe ND FDA UDI

Identifiers

Catalog Number
6669563 FDA UDI
Primary DI / UDI-DI
E27666695632 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dental guided surgery reference plate

CEREC Guide 3 by Sirona Dental Systems 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

Sources (1)

  • FDA UDI e6ad7ed0-37ee-4643-914d-e524769bfc1a 35 fields · synced May 30, 2026