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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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SILVERIN® — 15 UDI-DI variants, MDR (BANO Healthcare GmbH)

MD Atlas
BANO Healthcare GmbH

Data from EUDAMED, last updated May 23, 2026

SILVERIN®

9003527_SILVERIN_T6

15 UDI-DI variants

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

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

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 9003527_SILVERIN_T6
Device name: SILVERIN®
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: May 18, 2026

Manufacturer & authorised representative

Manufacturer

Name: BANO Healthcare GmbH
SRN: AT-MF-000000742
Country: Austria
Email: bano@bano.at
Phone: +432252823690

Variants by status

UDI-DI variants

15 UDI-DI variants

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Applied filters

basicUdiUlid01KRXN1MANSKQY3BK8VHHKV4KX

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

130465409003527136543
130463009003527136307
130467809003527136789
130464709003527136475
130416209003527131623
130412409003527131241
130415509003527131555
130411709003527131173
130414809003527131487
130417909003527131791
130413109003527131319
130422309003527132231
130421609003527132163
130423009003527132309
130427709003527132774