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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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WD4260 — 9 UDI-DI variants, MDR (Smeg S.p.A.)

MD Atlas
Smeg S.p.A.

Data from EUDAMED, last updated May 31, 2026

WD4260

8017709WD4260N7

9 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIb

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: Smeg S.p.A.

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 8017709WD4260N7
Device name: —
Device model: WD4260
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Apr 28, 2026

Manufacturer & authorised representative

Manufacturer

Name: Smeg S.p.A.
SRN: IT-MF-000019585
Country: Italy
Email: instruments@smeg.it
Phone: +39 0522 8211

Variants by status

UDI-DI variants

9 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KQA6962870N8ZCXJVT1K7329

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

MATLD6008017709309879
MTLD60-LC-00G08017709350581
TETHYSD6008017709309855
WD4260-DC-00008017709335809
WD4260-DC-00G08017709342739
WD4260-SC-00008017709321727
WD4260-SC-00G08017709324667
WD4260-SC-06008017709344306
WD4260-SC-06G08017709344290