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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 PURE — 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 PURE

85850746FM42U6

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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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 85850746FM42U6
Device name: DIAWIN D3 PURE
Device model: DIAWIN-D3-PURE
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 18, 2025

Manufacturer & authorised representative

Manufacturer

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

Variants by status

UDI-DI variants

45 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KCRENXG0VRKGC6GM66X27HVY

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

FM4236308585074602272
FM4242308585074602456
FM4248108585074602616
FM4245308585074602548
FM4249208585074602654
FM4240308585074602395
FM4244108585074602494
FM4242208585074602449
FM4236108585074602258
FM4248308585074602630
FM4242108585074602432
FM4250108585074602678
FM4244308585074602517
FM4238208585074602326
FM4250308585074602692
FM4239308585074602364
FM4237108585074602289
FM4240108585074602371
FM4239108585074602340
FM4250208585074602685

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