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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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Balto — 3 UDI-DI variants, MDR (Obseq B.V.)

MD Atlas
Obseq B.V.

Data from EUDAMED, last updated May 31, 2026

Balto

8720892BALTOZ9

3 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: Obseq B.V.

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 8720892BALTOZ9
Device name: —
Device model: Balto
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Special device type: refdata.special-mdr-device-type.software
Version date: Oct 17, 2025

Manufacturer & authorised representative

Manufacturer

Name: Obseq B.V.
SRN: NL-MF-000049636
Country: Netherlands
Email: alexander@obseq.nl

Variants by status

UDI-DI variants

3 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01K7S3FN41EF3HKXFVMC7PFPQ3

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

BALTO-WEB08720892824516
BALTO08720892824509
BALTO-APP-iOS08720892824523