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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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Cyber Ho - Litho Multicavity — 6 UDI-DI variants, MDR

MD Atlas
Quanta System S.p.A.

Data from EUDAMED, last updated May 31, 2026

Cyber Ho - Litho Multicavity

805917339FT2017-03JJ

6 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: Quanta System S.p.A.

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 805917339FT2017-03JJ
Device name: Cyber Ho - Litho Multicavity
Device model: Cyber Ho - Litho Multicavity
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Mar 30, 2026

Manufacturer & authorised representative

Manufacturer

Name: Quanta System S.p.A.
SRN: IT-MF-000007393
Country: Italy
Email: regulatory@quantasystem.com
Phone: +390331376797

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01KMZ1S6Z998W2B0R4ZHRSAZ4B

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

Cyber Ho 10008033945938932
Cyber Ho 15008059173391653
Cyber Ho 6008033945937508
Litho 10008033945938369
Litho 15008059173391738
Litho 6008033945937492