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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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Bedtime Antidekubitus — 1 UDI-DI variant, MDR (Bedtime AS)

MD Atlas
Bedtime AS

Data from EUDAMED, last updated May 30, 2026

Bedtime Antidekubitus

7072423000069TC

1 UDI-DI variant

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: Bedtime AS

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 7072423000069TC
Device name: Bedtime Antidekubitus
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 11, 2024

Manufacturer & authorised representative

Manufacturer

Name: Bedtime AS
SRN: NO-MF-000036284
Country: Norway
Email: post@sofies.no
Phone: +47 67 11 10 80

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01HV6DVSRSNZ9BCHDZ0Q9AX3HC

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

Bedtime Antidekubitus07072423000076