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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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Mini Vacuum — 3 UDI-DI variants, MDR (HOSPOTICA S.r.l.)

MD Atlas
HOSPOTICA S.r.l.

Data from EUDAMED, last updated May 31, 2026

Mini Vacuum

805803146MINIVACUUMCP

3 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIb

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: HOSPOTICA S.r.l.

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 805803146MINIVACUUMCP
Device name: Mini Vacuum
Device model: MV01
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Jul 24, 2025

Manufacturer & authorised representative

Manufacturer

Name: HOSPOTICA S.r.l.
SRN: IT-MF-000045987
Country: Italy
Email: info@hospotica.it
Phone: +39 06 83987351

Variants by status

UDI-DI variants

3 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01K0XTSRSCRH66RWXH3SMPXXA5

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

MV03-SMD03 08058031460029
MV0108058031460005
MV 02-MOOD08058031460012