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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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TomoCon GO — 1 UDI-DI variant, MDD (TatraMed Software s.r.o.)

MD Atlas
TatraMed Software s.r.o.

Data from EUDAMED, last updated May 30, 2026

TomoCon GO

B-TGO-2-EN

1 UDI-DI variant

MDD [Directive 93/42/EEC on medical devices]Class I

Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class I
Manufacturer: TatraMed Software s.r.o.

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Device characteristics

Active deviceMeasuring function

Legacy certificates

Certificate number: 2019-MDD/QS-032
Type: refdata.legacy.mdd-certificate-type.vi
Notified body: 3EC International a.s. (2265)
Validity: Apr 24, 2024

Identity & classification

Basic UDI-DI: B-TGO-2-EN
Device name: TomoCon GO
Device model: TomoCon GO - versions 1.0, 2.0, 2.1, 2.2, 2.3, 2.4
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class I
Special device type: refdata.special-mdd-device-type.software
Version date: Jan 10, 2024

Manufacturer & authorised representative

Manufacturer

Name: TatraMed Software s.r.o.
SRN: SK-MF-000017681
Country: Slovakia
Email: info@tatramed.sk
Phone: +421 2 6020 2301

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01GTHHZS3942JWWNRCMXBDXTJW

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

TomoCon GOD-TGO-2-EN