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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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b-box plus (DANAI) — 3 UDI-DI variants, MDR (b-rayZ AG)

MD Atlas
b-rayZ AG

Data from EUDAMED, last updated May 23, 2026

b-box plus (DANAI)

7649991532bboxplus2xxEU

3 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: b-rayZ AG

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 7649991532bboxplus2xxEU
Device name: b-box plus (DANAI)
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Special device type: refdata.special-mdr-device-type.software
Version date: Mar 5, 2024

Manufacturer & authorised representative

Manufacturer

Name: b-rayZ AG
SRN: CH-MF-000020036
Country: Switzerland
Email: cristina.rossi@b-rayz.ch

Authorised representative

Name: MED-RAS GmbH Regulatory Affairs Service
SRN: DE-AR-000006211
Country: Germany
Phone: +49 4104 9944440

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01HR726K38KKTVEZ9R17SVR77Z

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

b-box plus(DANAI)07649991532034
b-box plus(DANAI) ver. 2.2.007649991532072
b-box plus (DANAI)07649991532027