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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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Go product family — 17 UDI-DI variants, MDR (thego.care SAS)

MD Atlas
thego.care SAS

Data from EUDAMED, last updated May 19, 2026

Go product family

376043694GoFamily8Z

17 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: thego.care SAS

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 376043694GoFamily8Z
Device name: Go product family
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Aug 25, 2025

Manufacturer & authorised representative

Manufacturer

Name: thego.care SAS
SRN: FR-MF-000039697
Country: France
Email: contact@thego.care

Variants by status

UDI-DI variants

17 UDI-DI variants

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Applied filters

basicUdiUlid01K3G449NP9WX94BP582ME1Q4Z

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

23SC--LBKG03760436940086
23SC--MBKG03760436940093
23SC--SBKG03760436940109
23SC--LPNG03760436940123
23SC--MPNG03760436940130
23SC--SPNG03760436940147
23DD--LBKG03760436940048
23DD--MBKG03760436940017
23DD--SBKG03760436940024
23DD-XSBKG03760436940031
23DD--LPNG03760436940000
23DD--MPNG03760436940055
23DD--SPNG03760436940062
23DD-XSPNG03760436940079
23WL--LBLL03760436940161
23WL--MBLL03760436940178
23WL--SBLL03760436940185