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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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Standard — 254 UDI-DI variants, MDR (Mikai s.p.a.)

MD Atlas
Mikai s.p.a.

Data from EUDAMED, last updated May 31, 2026

Standard

805573143BSS000STANDARDX7

254 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: Mikai s.p.a.

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Device characteristics

Implantable

Identity & classification

Basic UDI-DI: 805573143BSS000STANDARDX7
Device name: Standard
Device model: Vite BSS
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Apr 15, 2026

Manufacturer & authorised representative

Manufacturer

Name: Mikai s.p.a.
SRN: IT-MF-000030732
Country: Italy
Email: mikai@mikai.it
Phone: +39 010 30801

Variants by status

UDI-DI variants

254 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KP821DB4WW8M7PJKZA98Y740

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

BTR70090LST08055400678368
BTR70095CST08055400678573
BTR70095SST08055400678184
BTR70095LST08055400678375