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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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ICamRef — 4 UDI-DI variants, MDR (Imetric 4D Imaging Sarl)

MD Atlas
Imetric 4D Imaging Sarl

Data from EUDAMED, last updated May 23, 2026

ICamRef

7640243239311318569T

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: Imetric 4D Imaging Sarl

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 7640243239311318569T
Device name: ICamRef
Device model: ICamRef
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 14, 2026

Manufacturer & authorised representative

Manufacturer

Name: Imetric 4D Imaging Sarl
SRN: CH-MF-000048162
Country: Switzerland
Email: quality@imetric4d.com

Authorised representative

Name: Imetric 4D GmbH
SRN: DE-AR-000046628
Country: Germany

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01KP567A6G73K9787PM36PHWJC

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

ICR-46-23-14-0807640243230531
ICR-46-23-14-06-0807640243230920
ICR-46-23-14-06-0807640243230920
ICR-46-23-14-0807640243230531