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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 SERENE — 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 SERENE

85850746FF45T9

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: 85850746FF45T9
Device name: DIAWIN D3 SERENE
Device model: DIAWIN-D3-SERENE
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 15, 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

basicUdiUlid01KCHCN9H4VMKGV69J93KJTWHT

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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FF4542208585074600643
FF4548308585074600834
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FF4543108585074600667
FF4540308585074600599
FF4549208585074600858
FF4545108585074600728
FF4536308585074600476
FF4541308585074600629
FF4550208585074600889
FF4550308585074600896
FF4537308585074600506
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FF4539108585074600544
FF4547108585074600780
FF4539308585074600568
FF4546208585074600766
FF4543308585074600681
FF4547208585074600797
FF4542108585074600636
FF4542308585074600650

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