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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 Medical Basic — 3 UDI-DI variants, MDR (Bedtime AS)

MD Atlas
Bedtime AS

Data from EUDAMED, last updated May 30, 2026

Bedtime Medical Basic

7072423000001SA

3 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: Bedtime AS

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 7072423000001SA
Device name: Bedtime Medical Basic
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Aug 28, 2023

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

3 UDI-DI variants

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Applied filters

basicUdiUlid01H8XZJ970WXQZVDBDRAAW6TD5

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 Medical Basic 80x20007072423000052
Bedtime Medical Basic 85x20007072423000045
Bedtime Medical Basic Mattress07072423000007