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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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Explorer™ TWIN Module — 4 UDI-DI variants, MDR (macu4 AG)

MD Atlas
macu4 AG

Data from EUDAMED, last updated May 23, 2026

Explorer™ TWIN Module

76499883732P01TWIN9E

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: macu4 AG

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 76499883732P01TWIN9E
Device name: Explorer™ TWIN Module
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 20, 2023

Manufacturer & authorised representative

Manufacturer

Name: macu4 AG
SRN: CH-MF-000022125
Country: Switzerland
Email: support@macu4.com
Phone: +41 076 701 69 46

Authorised representative

Name: macu4 GmbH
SRN: DE-AR-000031566
Country: Germany
Phone: +49 (0)7531 58 475 14

Variants by status

UDI-DI variants

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01GQ7EY1879660EM32W1J8B1WR

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

764998837329907649988373299
764998837328207649988373282
764998837327507649988373275
764998837326807649988373268