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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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Augmenatation_Plunger — 6 UDI-DI variants, MDR (Silony Medical GmbH)

MD Atlas
Silony Medical GmbH

Data from EUDAMED, last updated May 23, 2026

Augmenatation_Plunger

4054896AUGPLUNGERF9

6 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: Silony Medical GmbH

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Device characteristics

Reusable

Identity & classification

Basic UDI-DI: 4054896AUGPLUNGERF9
Device name: Augmenatation_Plunger
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 20, 2026

Manufacturer & authorised representative

Manufacturer

Name: Silony Medical GmbH
SRN: DE-MF-000006463
Country: Germany
Email: info@silony-medical.com
Phone: +497117825250

Variants by status

UDI-DI variants

6 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KS3G00MTNBPNWFEDZKVEZFXD

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

VERTICALE04054896090054
VERTICALE04054896031279
VERTICALE04054896005836
VERTICALE04054896090412
VERTICALE04054896031262
VERTICALE04054896090405