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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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Blåappen — 1 UDI-DI variant, MDR (Stretch Care AB)

MD Atlas
Stretch Care AB

Data from EUDAMED, last updated May 30, 2026

Blåappen

735012568Blaappen79

1 UDI-DI variant

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Stretch Care AB

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 735012568Blaappen79
Device name: Blåappen
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Sep 13, 2023

Manufacturer & authorised representative

Manufacturer

Name: Stretch Care AB
SRN: SE-MF-000007735
Country: Sweden
Email: daniel.terborn@stretch.se

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01HA6MHNKBZ6CY1Z9E83N2EVMT

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

Amni Care07350125680148