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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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Pedicle Rod (Carbon/PEEK, Ta marker) — 26 UDI-DI variants, MDR

MD Atlas
icotec ag

Data from EUDAMED, last updated May 23, 2026

Pedicle Rod (Carbon/PEEK, Ta marker)

764017255PSIRODBA00188

26 UDI-DI variants

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

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

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Device characteristics

Implantable

Identity & classification

Basic UDI-DI: 764017255PSIRODBA00188
Device name: Pedicle Rod (Carbon/PEEK, Ta marker)
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Apr 22, 2024

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

26 UDI-DI variants

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Applied filters

basicUdiUlid01HW2FH4XEP2TBJREZTEMX2Y5Z

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

No registered UDI-DI variants for this device family.