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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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Clef de serrage Scorpion — 4 UDI-DI variants, MDR (SCORPION)

MD Atlas
SCORPION

Data from EUDAMED, last updated May 19, 2026

Clef de serrage Scorpion

3770004158CLEFST8

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: SCORPION

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 3770004158CLEFST8
Device name: Clef de serrage Scorpion
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 14, 2021

Manufacturer & authorised representative

Manufacturer

Name: SCORPION
SRN: FR-MF-000000158
Country: France
Email: contact@scorpion.fr
Phone: +33 4 73 78 20 87

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01FPWPYZG2QANTX2WV6R8ZY6Z1

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

CLEF-EM Scorpion03770004158096
CLEF-KP Scorpion03770004158201
CLEF-SA Scorpion03770004158034
CLEF-SI Scorpion03770004158164