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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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Balancer — 2 UDI-DI variants, MDR (Focal Meditech BV)

MD Atlas
Focal Meditech BV

Data from EUDAMED, last updated May 30, 2026

Balancer

87193276493FOCBA1LM

2 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: Focal Meditech BV

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 87193276493FOCBA1LM
Device name: Balancer
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 24, 2022

Manufacturer & authorised representative

Manufacturer

Name: Focal Meditech BV
SRN: NL-MF-000000536
Country: Netherlands
Email: info@focalmeditech.nl
Phone: +31135333103

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01FT5WFXSP13ZTC9C4T3SK5AY8

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

60023608719327649329
60023508719327649336