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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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PUREKIT — 4 UDI-DI variants, MDR (TEKNIMED SAS)

MD Atlas
TEKNIMED SAS

Data from EUDAMED, last updated May 19, 2026

PUREKIT

376017704B33D7

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

No device characteristics flagged

Identity & classification

Basic UDI-DI: 376017704B33D7
Device name: PUREKIT
Device model: Mixing and injection system for bone cement
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 7, 2026

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

basicUdiUlid01GY9R66VN7VGJ024V494YN2Y4

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

T06042503760177045217
T06042603701505801075
T06042803701505801099
T06042703701505801082