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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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Dilator — 4 UDI-DI variants, MDR (icotec ag)

MD Atlas
icotec ag

Data from EUDAMED, last updated May 23, 2026

Dilator

764017255iPSI0009B6

4 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: icotec ag

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Device characteristics

Reusable

Identity & classification

Basic UDI-DI: 764017255iPSI0009B6
Device name: —
Device model: Dilator
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Apr 4, 2026

Manufacturer & authorised representative

Manufacturer

Name: icotec ag
SRN: CH-MF-000026833
Country: Switzerland
Email: RA@icotec.ch

Authorised representative

Name: icotec Medical GmbH
SRN: DE-AR-000016837
Country: Germany
Phone: +49 6171 708 59 07

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01KNBW9RGXYW14JJF08NT584PK

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

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VADER® Pedicle System Dilator Ø 19.5 mm07640164844343
VADER® Pedicle System Dilator Ø 7.0 mm07640164844312