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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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SD devices — 4 UDI-DI variants, MDR (Micromed S.p.A.)

MD Atlas
Micromed S.p.A.

Data from EUDAMED, last updated May 30, 2026

SD devices

803392812TD-SD9K

4 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: Micromed S.p.A.

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 803392812TD-SD9K
Device name: SD devices
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Apr 27, 2026

Manufacturer & authorised representative

Manufacturer

Name: Micromed S.p.A.
SRN: IT-MF-000009983
Country: Italy
Email: micromed.it@natus.com
Phone: +39 041 5937000

Variants by status

UDI-DI variants

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KQ6YB33D7W3XSFYQ6EGYJY9R

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

(01)0803392812194808033928121948
(01)0803392812195508033928121955
(01)0803392812188708033928121887
(01)0803392812193108033928121931