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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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Redsense Clamp System — 1 UDI-DI variant, MDR (Redsense Medical AB)

MD Atlas
Redsense Medical AB

Data from EUDAMED, last updated May 30, 2026

Redsense Clamp System

7350078030373X2

1 UDI-DI variant

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: Redsense Medical AB

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 7350078030373X2
Device name: Redsense Clamp System
Device model: Redsense Clamp System
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 5, 2025

Manufacturer & authorised representative

Manufacturer

Name: Redsense Medical AB
SRN: SE-MF-000005240
Country: Sweden
Email: info@redsensemedical.com
Phone: +46 35 1060 30

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01JKAQT8BCKFANQ1PBXJ8WY6K9

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

Redsense Clamp System07350078030373