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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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ROLLATOR — 2 UDI-DI variants, MDR (Ebizlab srl)

MD Atlas
Ebizlab srl

Data from EUDAMED, last updated May 31, 2026

ROLLATOR

805609ROLLP9

2 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: Ebizlab srl

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805609ROLLP9
Device name: —
Device model: ROLLATOR
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 11, 2025

Manufacturer & authorised representative

Manufacturer

Name: Ebizlab srl
SRN: IT-MF-000046729
Country: Italy
Email: guglielmo.longobucco@ebizlab.it

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01JRJN21A06PDGCYESY6Z6S7GM

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

2899608056090285140
3713508056090485953