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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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Termodisinfettore 10-12 DIN — 5 UDI-DI variants, MDR (Smeg S.p.A.)

MD Atlas
Smeg S.p.A.

Data from EUDAMED, last updated May 31, 2026

Termodisinfettore 10-12 DIN

8017709WD6010MU

5 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: 8017709WD6010MU
Device name: —
Device model: Termodisinfettore 10-12 DIN
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: May 5, 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

5 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KQVTD6GF7N7TF0MKJEMBZAKH

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

WD601008017709201722
WD6010M08017709201692
WD6010M308017709254193
WD6010T08017709201708
WD6010TM08017709201715