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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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- — 3 UDI-DI variants, MDR (sfm medical devices GmbH)

MD Atlas
sfm medical devices GmbH

Data from EUDAMED, last updated May 23, 2026

-

406357490018AK

3 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: sfm medical devices GmbH

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Device characteristics

Administers medicine

Identity & classification

Basic UDI-DI: 406357490018AK
Device name: -
Device model: nextaro® va
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jul 12, 2024

Manufacturer & authorised representative

Manufacturer

Name: sfm medical devices GmbH
SRN: DE-MF-000008166
Country: Germany
Email: regulatory@sfm.de
Phone: +49 6053 805 0

Variants by status

UDI-DI variants

3 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01HQ8EYX03K6E83ZHVC1DNCS0Z

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

8835504063574200296
nextaro® va, 13mm, 5µm04063574200425
2003704063574200371