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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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Zitzi Delfi — 2 UDI-DI variants, MDR (Anatomic Sitt i Norrköping AB)

MD Atlas
Anatomic Sitt i Norrköping AB

Data from EUDAMED, last updated May 30, 2026

Zitzi Delfi

732247DelfiMC

2 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: Anatomic Sitt i Norrköping AB

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 732247DelfiMC
Device name: Zitzi Delfi
Device model: Modular seating system
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 1, 2021

Manufacturer & authorised representative

Manufacturer

Name: Anatomic Sitt i Norrköping AB
SRN: SE-MF-000002240
Country: Sweden
Email: info@anatomicsitt.com
Phone: +46 (0)11 16 18 00

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01FMMAJA84NGAJ9MBFA2Y1X9VH

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

Armrest cup. size 1 (Base/325mm) - Delfi07322472857610
Seat size 0 - Zitzi Delfi Pro07322472840100