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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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UpRise Støttestang — 5 UDI-DI variants, MDR (Bedtime AS)

MD Atlas
Bedtime AS

Data from EUDAMED, last updated May 30, 2026

UpRise Støttestang

07072423000083CQ

5 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: 07072423000083CQ
Device name: UpRise Støttestang
Device model: UpRise Støttestang
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 4, 2025

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

5 UDI-DI variants

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Applied filters

basicUdiUlid01JK7Z4BYWXXQDY3FSD7J58X4Z

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

B-UR100307072423000120
B-UR100207072423000113
BS12407072423000137
B-UR100007072423000090
B-UR100107072423000106