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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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ModuDosing Rectal Lead — 2 UDI-DI variants, MDR (Modulpac AB)

MD Atlas
Modulpac AB

Data from EUDAMED, last updated May 31, 2026

ModuDosing Rectal Lead

735014394RECTCB

2 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: Modulpac AB

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Device characteristics

Administers medicine

Identity & classification

Basic UDI-DI: 735014394RECTCB
Device name: ModuDosing Rectal Lead
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 19, 2026

Manufacturer & authorised representative

Manufacturer

Name: Modulpac AB
SRN: SE-MF-000024685
Country: Sweden
Email: order@modulpac.se
Phone: +4637225500

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01KS03K67QPSSKRV8A3QNPQ1X4

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

804000400217350143940016
804000400107350143940019