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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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Folding — 118 UDI-DI variants, MDR (Etac Supply Center AB)

MD Atlas
Etac Supply Center AB

Data from EUDAMED, last updated May 31, 2026

Folding

732045104049

118 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: Etac Supply Center AB

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 732045104049
Device name: —
Device model: Folding
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 2, 2025

Manufacturer & authorised representative

Manufacturer

Name: Etac Supply Center AB
SRN: SE-MF-000001230
Country: Sweden
Email: info@etac.com
Phone: +46 371 587200

Variants by status

UDI-DI variants

118 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01K6HQTBY0P23WG1K11P0RVZFV

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

Cross 607320451417336
Cross 607320451478092
Cross 607320451477958
Cross 607320451417343
Cross 607320451417312
Cross 607320451478047
Cross 607320451417299
Cross 607320451450418
Cross 607320451478214
Cross 607320451444066
Cross 607320451444059
Cross 607320451438249
Cross 607320451478061
Cross 607320451417237
Cross 607320451478030
Cross 607320451450500
Cross 607320451450470
Cross 607320451450487

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