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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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Reflex Hammer — 11 UDI-DI variants, MDR (Luxamed GmbH & Co. KG)

MD Atlas
Luxamed GmbH & Co. KG

Data from EUDAMED, last updated May 23, 2026

Reflex Hammer

426038196ReflexhammerC6

11 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: Luxamed GmbH & Co. KG

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426038196ReflexhammerC6
Device name: Reflex Hammer
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jul 6, 2022

Manufacturer & authorised representative

Manufacturer

Name: Luxamed GmbH & Co. KG
SRN: DE-MF-000006437
Country: Germany
Email: info@luxamed.de
Phone: 07344/9290510

Variants by status

UDI-DI variants

11 UDI-DI variants

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Applied filters

basicUdiUlid01G79M029C0WDRTXYYZ8JQXKQ0

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

M1.131.41404260381965268
M1.121.81204260381960256
M1.121.11204260381960249
M1.121.31204260381963721
M1.121.41204260381963714
M1.111.11204260381960287
M1.121.51304260381960263
M1.111.91504260381960317
M1.131.91404260381963356
M1.121.91404260381960270
M1.121.61204260381963691