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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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BINAMED Silbertextilien — 19 UDI-DI variants, MDR (Binamed Moll GmbH)

MD Atlas
Binamed Moll GmbH

Data from EUDAMED, last updated May 31, 2026

BINAMED Silbertextilien

426017207SilbertexBP

19 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: Binamed Moll GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426017207SilbertexBP
Device name: BINAMED Silbertextilien
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 29, 2026

Manufacturer & authorised representative

Manufacturer

Name: Binamed Moll GmbH
SRN: DE-MF-000032697
Country: Germany
Email: info@binamed.de
Phone: +4992174590

Variants by status

UDI-DI variants

19 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KSHHJJY6Y7H2HDD79KDE2MWQ

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

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90030204260172073028
90140004260172073127
90140104260172073134
90140204260172073141
90140304260172073158
90070104260172073059
90070204260172073066
90070004260172073042
90070304260172073073
90225104260172073172
90225004260172073165
90080104260172073097
90080004260172073080
90080304260172073110
90080204260172073103
91011004260172073189
90030004260172073004
90030104260172073011