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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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Cases and Trays — 4 UDI-DI variants, MDR (TEKNIMED SAS)

MD Atlas
TEKNIMED SAS

Data from EUDAMED, last updated May 19, 2026

Cases and Trays

376017704B31D3

4 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: TEKNIMED SAS

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Device characteristics

Reusable

Identity & classification

Basic UDI-DI: 376017704B31D3
Device name: —
Device model: Cases and Trays
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Sep 14, 2023

Manufacturer & authorised representative

Manufacturer

Name: TEKNIMED SAS
SRN: FR-MF-000001224
Country: France
Email: teknimed@teknimed.com

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01FKJN7NJE6R3GH94TAN2R5CPE

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

T06729403760177049963
T06729103760177049932
T067292 03760177049949
T067799 03760177040311