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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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BOTTICELLI — 56 UDI-DI variants, MDR (FERROX srl)

MD Atlas
FERROX srl

Data from EUDAMED, last updated May 31, 2026

BOTTICELLI

805347043BOTTICELLI8K

56 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: FERROX srl

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 805347043BOTTICELLI8K
Device name: BOTTICELLI
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 30, 2026

Manufacturer & authorised representative

Manufacturer

Name: FERROX srl
SRN: IT-MF-000011243
Country: Italy
Email: info@ferrox.it
Phone: 0438777099

Variants by status

UDI-DI variants

56 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KMZHE247CMAW3CGXVRS51YJ8

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

238000R.2308052532970001
238000.3008053470430688
238000.1708053470430664
238000.308052532973651
238000.3108053470430695
238000.808053470430749

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