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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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Hoist — 6 UDI-DI variants, MDR (Sunrise Medical GmbH)

MD Atlas
Sunrise Medical GmbH

Data from EUDAMED, last updated May 23, 2026

Hoist

4050063hoistF8

6 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: Sunrise Medical GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 4050063hoistF8
Device name: Hoist
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Sep 12, 2022

Manufacturer & authorised representative

Manufacturer

Name: Sunrise Medical GmbH
SRN: DE-MF-000006320
Country: Germany
Email: kundenservice@sunrisemedical.de
Phone: +4972539800

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01GCS0S02QK7T3QX03YB2P3SAZ

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

G130E04050063045001
G15004050063042994
MICRO04050063060141
Sunlift Slings04050063045018
G17504050063044981
G165LI04050063060950