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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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Insert — 2 UDI-DI variants, MDR (Attends Healthcare AB)

MD Atlas
Attends Healthcare AB

Data from EUDAMED, last updated May 31, 2026

Insert

7332152358179G

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: Attends Healthcare AB

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 7332152358179G
Device name: Insert
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 6, 2026

Manufacturer & authorised representative

Manufacturer

Name: Attends Healthcare AB
SRN: SE-MF-000002628
Country: Sweden
Email: info@attends.se

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01KQY9YG3FZA4SGD5B29BJCY5C

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

733215220010007332152200087
733215220009407332152200070