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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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FF4546108585074600759
FF4545208585074600735
FF4537208585074600490
FF4540208585074600582
FF4544208585074600704
FF4538308585074600537
FF4536108585074600452
FF4547308585074600803
FF4549308585074600865
FF4546308585074600773
FF4538208585074600520
FF4541108585074600605
FF4540108585074600575
FF4548208585074600827
FF4545308585074600742
FF4541208585074600612
FF4543208585074600674
FF4549108585074600841
FF4544108585074600698

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