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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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Trocar Needle CH 7 — 4 UDI-DI variants, MDR (Redax S.p.A.)

MD Atlas
Redax S.p.A.

Data from EUDAMED, last updated May 31, 2026

Trocar Needle CH 7

803413929NEEDLE1aS5

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: Redax S.p.A.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 803413929NEEDLE1aS5
Device name: Trocar Needle CH 7
Device model: Trocar Needle CH 7
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Apr 22, 2026

Manufacturer & authorised representative

Manufacturer

Name: Redax S.p.A.
SRN: IT-MF-000019320
Country: Italy
Email: gianluca.boni@redax.it

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01KPT4HXQNR37X0D0BDY22TZRG

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

2300208034139294278
2300308034139294285
2300408034139294292
2300608034139294308