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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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Human Smart Safe Therapy — 2 UDI-DI variants, MDR (BIMIND SRL)

MD Atlas
BIMIND SRL

Data from EUDAMED, last updated May 31, 2026

Human Smart Safe Therapy

805620907HVDSST1RM

2 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: BIMIND SRL

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 805620907HVDSST1RM
Device name: Human Smart Safe Therapy
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Special device type: refdata.special-mdr-device-type.software
Version date: Mar 21, 2025

Manufacturer & authorised representative

Manufacturer

Name: BIMIND SRL
SRN: IT-MF-000028042
Country: Italy
Email: amministrazione@bimind.it
Phone: +39 0731 696134

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01JPWTSCS840BETPAMVH2Q5R2C

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

Human Smart Safe Therapy08056209070001
Human Smart Safe Therapy08056209070018