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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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DIAWIN D3 NOIR — 45 UDI-DI variants, MDR (Diawin s.r.o.)

MD Atlas
Diawin s.r.o.

Data from EUDAMED, last updated May 31, 2026

DIAWIN D3 NOIR

85850746FM41U4

45 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: Diawin s.r.o.

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UDI-DI variants

45 UDI-DI variants

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Applied filters

basicUdiUlid01KCNR3EMJC8Z679H42X7BVNFB

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

FM4141108585074601954
FM4143308585074602036
FM4140108585074601923
FM4149208585074602203
FM4142308585074602005
FM4146108585074602104
FM4148308585074602180
FM4136308585074601824
FM4143208585074602029
FM4136208585074601817
FM4139308585074601916
FM4148108585074602166
FM4149308585074602210
FM4136108585074601800
FM4138308585074601886
FM4138108585074601862
FM4142108585074601985
FM4146208585074602111
FM4147308585074602159
FM4138208585074601879

1 2

Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 85850746FM41U4
Device name: DIAWIN D3 NOIR
Device model: DIAWIN-D3-NOIR
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 17, 2025

Manufacturer & authorised representative

Manufacturer

Name: Diawin s.r.o.
SRN: SK-MF-000048596
Country: Slovakia
Email: janura@diawin.de

Variants by status