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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Zfx® Intraoral Scanbody — 32 UDI-DI variants, MDR (Zfx GmbH)

MD Atlas
Zfx GmbH

Data from EUDAMED, last updated May 23, 2026

Zfx® Intraoral Scanbody

42518817-AM-I-Scanbody-YW

32 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: Zfx GmbH

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Device characteristics

Reusable

Identity & classification

Basic UDI-DI: 42518817-AM-I-Scanbody-YW
Device name: Zfx® Intraoral Scanbody
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 13, 2026

Manufacturer & authorised representative

Manufacturer

Name: Zfx GmbH
SRN: DE-MF-000018101
Country: Germany
Email: qm@zfx-dental.com
Phone: +49 81313324420

Variants by status

UDI-DI variants

32 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KP3AJR9PKGTRN31KHCD9D1Q7

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

ZFX0500192604251881760767
ZFX0500192904251881760828
ZFX0500194704251881763249
ZFX0500196104251881763386
ZFX0500195104251881763287
ZFX0500194604251881761122
ZFX0500196204251881761283

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